Categories
Herbs & Plants

Showy Milkweed

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Botanical Name :Asclepias speciosa
Family: Apocynaceae
Subfamily: Asclepiadoideae
Genus: Asclepias
Species: A. speciosa
Kingdom: Plantae
Order: Gentianales

Common Names: Showy Milkweed, Greek Milkweed(don’t ask me) and Common Milkweed.

Habitat :It is native to the western half of North America.Showy milkweed is widespread  throughout the western states from Texas north to  British Columbia.

Description:
This flowering plant is a hairy, erect perennial. The large, pointed, bananalike leaves are arranged opposite on the stalklike stem. The eye-catching furry pale pink to pinkish-purple flowers are arranged in thick umbels. Their corollas are reflexed and the central flower parts, five hoods with prominent hooks, are star-shaped. The fruit is a large, rough follicle filled with many flat oval seeds with luxuriant silky plumes.
Click to see the pictures…...(01)....(1)……..(2).……..(3)..…....(4).….(5).
Thriving in poor, dry , well-drained soil, it’s tough and vigorous with gorgeous large silvery-green, soft-to-the-touch leaves. Atop the 3′ to 4′ stems, the remarkably FRAGRANT large round clusters are 4″ to 5″ across and made up of lovely velvety pink and white star-like flowers. Bloom season occurs late Spring to late Summer.

Asclepias speciosa is a specific Monarch butterfly food and habitat plant.

Many Native American peoples use all parts of this plant for a great number of medicinal uses and ate some parts as a food.

Cultivation:
It needs sun. It is quite drought tolerant,(not in the same league though as Asclepias A. eriocarpa, erosa or californica ) plant, water well first summer and ignore. Tolerates alkaline soils and most gardens. Needs cross-pollination for fruit and seed development.

Pollen is self-incompatible alkaloids associated with this plant give the butterflies that feed on it protection. The alkaloids associated with this plant give the butterflies that feed on it protection.

Propagation :
Reproduction occurs from seed, roots that spread horizontally and send up new shoots, and from severed pieces of root. Each plant can produce from hundreds to thousands of seeds. Growth nodes occur along the roots, and each node can produce a new plant. The silky, feathery exterior of the seed facilitates spread by both water and wind. The seed attachment also clogs screens of combines during harvest.

Chemical Constituents:
Three chemicals have proven effective on showy milkweed: 1) amitrole (Amizol-T); 2) picloram (Tordon); and 3) glyphosate (Roundup). 2,4-D can be mixed with the  picloram and  glyphosate.

Edible Uses:

The young shoots, stems, flower buds, immature fruits, and roots of showy milkweed were boiled and eaten as a vegetable by various indigenous groups of eastern and mid-western America.
In some areas the young leaves and stems were used as greens. The flowers were also eaten raw or boiled, and the buds were boiled for soup or with meat. The most common use for these plants, recorded among almost all the tribes throughout California, was to obtain a kind of chewing gum from the sap of Asclepias speciosa. The sticky white sap was heated slightly until it became solid, then added to salmon fat or deer grease.

Pueblo people ate green milkweed pods and uncooked roots from one of the species that forms fleshy tubers underground.

Medicinal Uses;
The sap of Asclepias speciosa was used as a cleansing and healing agent by some of the desert tribes for sores, cuts, and as a cure for warts and ringworm. The silky hairs were burned off the ripe seeds, which were then ground and made into a salve for sores. Seeds were boiled in a small amount of water and the liquid used to soak rattlesnake bites to draw out the poison. A hot tea made from the roots was given to bring out the rash in measles or as a cure for coughs. It was also employed as a wash to cure rheumatism. The mashed root, moistened with water, was used as a poultice to reduce swellings.


Other Uses:

Fibers from the stems of milkweed have been identified in prehistoric textiles in the Pueblo region. Tewa-speaking people of the Rio Grande still make string and rope from these fibers. At Zuni, the silky seed fibers are spun on a hand-held wooden spindle and made into yarn and woven into fabric, especially for dancers.

Known Hazards:
There are reports that it is increasing in abundance throughout parts of its range. Showy milkweed is a plant of concern because it can be toxic to sheep, cattle, horses and domestic fowl. It is most toxic during rapid growth, but retains its toxicity when dried in hay. Fast growth occurs when temperatures are warm and soil moisture is abundant.

Disclaimer:
The information presented herein is intended for educational purposes only. Individual results may vary, and before using any supplements, it is always advisable to consult with your own health care provider.

Resources:
http://en.wikipedia.org/wiki/Asclepias_speciosa
http://www.anniesannuals.com/plt_lst/lists/general/lst.gen.asp?prodid=125
http://www.laspilitas.com/nature-of-california/plants/asclepias-speciosa

Click to access FS0360.pdf

Click to access cs_assp.pdf

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Categories
Ailmemts & Remedies

Amyloidosis

Alternative Names: Amyloid – primary

Definition:
In medicine, amyloidosis refers to a variety of conditions in which amyloid proteins are abnormally deposited in organs and/or tissues. A protein is described as being amyloid if, due to an alteration in its secondary structure, it takes on a particular aggregated insoluble form similar to the beta-pleated sheet.  Symptoms vary widely depending upon the site of amyloid deposition. Amyloidosis may be inherited or acquired.

CLICK & SEE THE PICTURES

The collection of these abnormal proteins interferes with the normal functioning of the organ affected.

Since there are more than 20 different proteins that may form amyloid, there are also many different types of amyloidosis.

Classification of amyloid:
The modern classification of amyloid disease tends to use an abbreviation of the protein that makes the majority of deposits, prefixed with the letter A. For example amyloidosis caused by transthyretin is termed “ATTR.” Deposition patterns vary between patients but are almost always composed of just one amyloidogenic protein. Deposition can be systemic (affecting many different organ systems) or organ-specific. Many amyloidoses are inherited, due to mutations in the precursor protein. Other forms are due to different diseases causing overabundant or abnormal protein production – such as with over production of immunoglobulin light chains in multiple myeloma (termed AL amyloid), or with continuous overproduction of acute phase proteins in chronic inflammation (which can lead to AA amyloid).

Out of the approximately 60 amyloid proteins that have been identified so far,  at least 36 have been associated in some way with a human disease.

Amyloidosis is rare, being diagnosed in between one and five in every 100,000 people every year. It’s more common in older people and is also slightly more common in men than in women.

Causes:
The cause of primary amyloidosis is unknown, but the condition is related to abnormal production of antibodies by a type of immune cell called plasma cells.

The symptoms depend on the organs affected by the deposits. These organs can include the tongue, intestines, skeletal and smooth muscles, nerves, skin, ligaments, heart, liver, spleen, and kidneys.

Primary amyloidosis can result in conditions that include:

•Carpal tunnel syndrome
•Gastrointestinal reflux (GERD)
•Heart muscle damage (cardiomyopathy)
•Kidney failure
•Malabsorption
The deposits build up in the affected organs, causing them to become stiff, which decreases their ability to function.

Risk factors have not been identified. Primary amyloidosis is rare. It is similar to multiple myeloma, and is treated the same way.

Symptoms:

CLICK & SEE
•Enlarged tongue
•Fatigue
•Irregular heart rhythm
•Numbness of hands and feet
•Shortness of breath
•Skin changes
•Swallowing difficulties
•Swelling in the arms and legs
•Weak hand grip
•Weight loss

Additional symptoms that may be associated with this disease:
•Clay-colored stools
•Decreased urine output
•Diarrhea
•Hoarseness or changing voice
•Joint pain
•Other tongue problems
•Weakness

CLICK TO SEE THE STAGES

Diagnosis:
Exams and Tests
Your doctor may discover that you have an enlarged liver or spleen.

If specific organ damage is suspected, your doctor may order tests to confirm amyloidosis of that organ. For example:

•Abdominal ultrasound may reveal a swollen liver or spleen.
•An abdominal fat pad biopsy, rectal mucosa biopsy, or a bone marrow biopsy can help confirm the diagnosis.
•A heart evaluation, including an ECG,may reveal arrhythmias, abnormal heart sounds, or signs of congestive heart failure. An echocardiogram shows poor motion of the heart wall, due to a stiff heart muscle.
•A carpal tunnel syndrome evaluation may show that hand grips are weak.Nerve conduction velocity shows abnormalities.
•Kidney function tests may show signs of kidney failure or too much protein in the urine ( nephrotic syndrome).
?BUN level is increased.
?Serum creatinine is increased.
?Urinalysis shows protein, casts, or fat bodies.

This disease may also alter the results of the following tests:
•Bence-Jones protein (quantitative)
•Carpal tunnel biopsy
•Gum biopsy
•Immunoelectrophoresis – serum
•Myocardial biopsy
•Nerve biopsy
•Quantitative immunoglobulins
•Tongue biopsy
•Urine protein

Treatment:
It isn’t always easy to treat amyloidosis, and there is no treatment yet that specifically targets the amyloid depositing in the tissues. In cases where it’s secondary to another problem (AA amyloidosis), such as rheumatoid arthritis, treating that original problem may stop the progress of amyloidosis or may even reverse it.

In cases of primary amyloidosis (AL amyloidosis), chemotherapy drugs may be given to suppress production of new amyloid and cause regression of existing amyloid deposits.

In secondary amyloidosis, aggressive treatment of the underlying disease can improve symptoms and/or slow progression of disease. Complications such as heart failure, kidney failure, and other problems can sometimes be treated as necessary.

Occasionally, transplantation of a damaged organ is necessary. However, even after this has been carried out the new organ may become affected by amyloidosis.

Treatment may also be aimed at supporting the function of damaged tissues and treating complications such as heart or kidney failure.

Overall, many types of amyloidosis follow a steadily progressive course and may prove fatal within a year or two.

Prognosis :
The severity of the disease depends upon the organs affected. Heart and kidney involvement may lead to organ failure and death. Systemic involvement is associated with death within 1 to 3 years.

Possible Complications:
•Congestive heart failure
•Death
•Endocrine failure (hormonal disorder)
•Kidney failure
•Respiratory failure

Prevention : There is no known prevention.

Disclaimer: This information is not meant to be a substitute for professional medical advise or help. It is always best to consult with a Physician about serious health concerns. This information is in no way intended to diagnose or prescribe remedies.This is purely for educational purpose.

Resources:
http://www.bbc.co.uk/health/physical_health/conditions/amyloidosis1.shtml
http://www.nlm.nih.gov/medlineplus/ency/article/000533.htm
http://en.wikipedia.org/wiki/Amyloidosis

http://health.allrefer.com/pictures-images/amyloidosis-on-the-face.html

http://health.allrefer.com/health/cardiac-amyloidosis-dilated-cardiomyopathy.html

http://morningreporttgh.blogspot.com/2010/04/amyloidosis.html

http://gsm.utmck.edu/research/HICP/overview.cfm

http://www.pathologyatlas.ro/amyloidosis-kidney-pathology.php

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Categories
Ailmemts & Remedies

Allergic Asthma

Definition:
Allergic (extrinsic) asthma is characterized by symptoms that are triggered by an allergic reaction. Allergic asthma is airway obstruction and inflammation that is partially reversible with medication. Allergic asthma is the most common form of asthma, affecting over 50% of the 20 million asthma sufferers.Over 2.5 million children under age 18 suffer from allergic asthma. Many of the symptoms of allergic and non-allergic asthma are the same (coughing, wheezing, shortness of breath or rapid breathing, and chest tightness). However, allergic asthma is triggered by inhaled allergens such as dust mite allergen, pet dander, pollen, mold, etc. resulting in asthma symptoms.

click & see the pictures
Allergies and asthma often occur together. The same substances that trigger your hay fever symptoms may also cause asthma signs and symptoms such as shortness of breath, wheezing and chest tightness. This is called allergic asthma or allergy-induced asthma. Substances such as pollen, dust mites and pet dander are common triggers. In some people, skin or food allergies can cause asthma symptoms.

An allergic response occurs when immune system chemicals (antibodies) mistakenly identify a harmless substance such as tree pollen as a dangerous invader. In an attempt to protect your body from the substance, antibodies attack the allergen. The chemicals released by your immune system lead to allergy signs and symptoms, such as nasal congestion, runny nose, itchy eyes or skin reactions. For some people, this same reaction also affects the lungs and airways, leading to asthma symptoms.

Symptoms:

The main symptoms are coughing, wheezing, shortness of breath and a tight feeling in the chest.

…...CLICK & SEE

Difference Between Allergy and non-Allergic Asthma:

Allergic asthma symptoms are similar to the non-allergy asthma ones. Both types of sufferers experience wheezing, coughing, chest tightness, chest pain or pressure, shortness of breath, sleep troubles. The early warning symptoms can be signs of frequent colds such as sneezing, sore throat, nasal congestion, running nose, or a permanent feeling of tiredness and bad mood. While both types of asthma manifest the same symptoms, the difference is made by the trigger of these symptoms. In case of allergic asthma, attacks are triggered by allergens such as pollens, pet dander, mold or dust. This is why all asthma sufferers need to be aware of their type of asthma, so they can apply preventive measures such as eating healthy foods and staying away from allergens. It is very important that allergic asthma sufferers try not to get in contact with the substances they are allergic to (allergens). These substances are easy to be determined by running some special tests, which any allergology lab can do.


Causes:

Asthma often runs in ‘atopic’ families. Children are also more likely to develop asthma if their mother smoked during pregnancy or while breastfeeding.

Most people find several things trigger their asthma. Some of the most common predisposing factors for asthma are allergies to:

•House dust mites
•Mould spores
•Pollen
•Pets
•Food or food preservatives

Asthma triggers include:

•Viral infections, such as colds and flu
•Cigarette smoke
•Certain forms of exercise, such as running
•Exposure to cold, dry air
•Laughing and other emotions
•Medication containing aspirin
•Drinks containing sulphur dioxide, such as squashes and lemon barley water

Treatment:
Some treatment can reduce both asthma and allergy symptoms, but most are designed to treat either one or the other. A few treatments can help with both conditions.

There are two main treatments for asthma:

•Relievers – salbutamol and terbutaline
•Preventers – beclomethasone, budesonide, fluticasone, mometasone and ciclesonide
These all come in a variety of delivery devices, such as aerosol or powder inhalers and nebulisers. You breathe the medicine in through your mouth, directly into your lungs.

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Relievers are drugs called bronchodilators (based on adrenaline) that relax the muscles which surround the airways, making it easier to breathe. You should take these as directed by your doctor as soon as symptoms appear.

Taking a dose of the reliever inhaler before exercise will increase your stamina and prevent breathing difficulty.

Preventers are drugs (usually low-dose steroids) that reduce inflammation in the airways and make them less sensitive. This means you’re less likely to react when exposed to a trigger.

The protective effect of this medicine is built up over a period of time, so you must take your preventer regularly, as directed by your doctor.

Combination preventer and long-acting reliever (formoterol and salmeterol) inhalers have become popular and seem to be particularly good at controlling more severe and persistent asthma.

If your asthma is really bad, your doctor may also prescribe a short course of steroid tablets to calm your inflamed airways.

Newer anti-inflammatory medication includes leukotriene receptor antagonists (montelukast and zafirlukast), which are particularly useful for brittle asthma and patients with aspirin-sensitive asthma.

The most recent addition to the list of possible treatments for asthma is a new injection medication (omalizumab) for those with severe allergic asthma, which works by dampening down the IgE allergic reaction.

An older orally administered bronchodilator, theophylline, isn’t often used these days owing to its unpredictable toxic side-effects and need for blood testing.

There is little scientific evidence to support the use of breathing exercises, such as Buteyko, in the treatment of asthma. However, some people with asthma find breathing exercises calm their symptoms and reduce their need for reliever medication.

You may need other medications to treat allergies or asthma, especially if your symptoms become severe at times. However, recognizing and avoiding the allergic substances that trigger your symptoms is the most important step you can take.

Who’s at risk of allergic asthma?
A family history of allergies is a major risk factor for allergic asthma. Having hay fever or other allergies yourself also increases your risk of getting asthma.

Allergic Asthma Preventive Measures:
If you’ve already been diagnosed with allery or allergic asthma, then you should also have a list of allergens you are sensitive to. It is not a joke, you need to stay away as much as you can from getting in contact with those allergens, if you want your allergic asthma not to bother you very often. Living a symptom-free life is possible in a big degree, but you need to understand how serious this allergic asthma issue has to be treated. Maybe this means that you’ll need to stay indoors in the days with high pollen activity, or maybe you won’t be allowed to eat strawberries again for the rest of your life. Understand that your lifestyle could change forever after you’ve found out that you suffer from allergy or allergic asthma.


Is all asthma caused by allergies?

Though allergic asthma is the one of the most common kinds of asthma, there are other types with different kinds of triggers. For example, for some people, asthma can be triggered by exercise, infections, cold air or gastroesophageal reflux disease (GERD). Many people have more than one kind of asthma trigger.

Pediatric Asthma
Pediatric asthma is one of the most delicate conditions that affect children of all ages. Before getting to the pediatric asthma treatment, we have to talk about the correct diagnosis, as this is a very hard thing to accomplish. Small children and infants cannot tell what bothers them, so the symptoms have to be guessed first by parents, and then by doctors. If a parent doesn’t suspect anything abnormal in their child, why would they seek for pediatric medical consultation? Children get frequent colds and childhood diseases, so there’s another reason for parents not getting too worried if their child coughs and has difficulties in breathing.

Can one prevent asthma?
You can help to avoid asthma attacks by taking preventer medicine regularly and avoiding your triggers. You can also monitor your asthma by asking your doctor to provide you with a peak flow meter, a simple device that measures the amount of breath in your lungs.

Most childhood asthma is caused by an allergy. Skin-prick and RAST tests may be able to discover the allergen. Practical steps can then be taken to avoid it, be it house dust mites, cats, dogs or other pets. Even mould spores and pollen grains can trigger seasonal asthma attacks.

If you’re prone to sudden or severe asthma attacks, keep asthma diary cards and a peak flow meter on hand to monitor your lung airflow so you can take early action.

Discuss an asthma action plan with your GP, who may issue an emergency supply of oral steroid pills. You may need to increase your medication dosage if your peak flow measurement drops steadily.

Remember, never stop taking your preventer medication, even when your symptoms are stable. Don’t wait until your symptoms get worse – they’ll be harder to treat.

By regular practicing Yoga  one can get rid of  Asthma totally

You may click to see :Yoga For Asthma Patients

You may click  for more informations  about Allergic Asthma :

Disclaimer: This information is not meant to be a substitute for professional medical advise or help. It is always best to consult with a Physician about serious health concerns. This information is in no way intended to diagnose or prescribe remedies.This is purely for educational purpose.

Resources:

http://understandingasthma.com/
http://www.bbc.co.uk/health/physical_health/conditions/in_depth/allergies/allergicconditions_asthma.shtml
http://inflation.us/collegebubble.html
http://www.mayoclinic.com/health/allergies-and-asthma/AA00045

http://www.aafa.org/display.cfm?id=9&sub=16

http://alltruthabouthealth.info/allergic-asthma-is-the-type-of-asthma-problem/

http://www.poandpo.com/in-sickness-and-health/bronchial-and-allergic-asthma/

http://seerpress.com/causes-of-allergic-asthma-revealed/5423/

http://healthguide.howstuffworks.com/exercise-induced-asthma-picture-a.htm

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News on Health & Science

Curcumin Relieves Pain and Inflammation for Osteoarthritis Patients

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A study shows that a formulation of curcumin can relieve pain and increase mobility in patients with osteoarthritis.  It can also reduce a series of inflammatory markers.
..CLICK & SEE
100 patients with osteoarthritis were divided in two groups — the first group was given the “best available treatment” and the second group was given the same treatment plus 200 mg of the curcumin formulation each day.

According to IFT:
“The results showed that the [curcumin]-treated group had a statistically significant reduction in all primary clinical end-points … These results were complemented by the evaluation of a series of inflammatory markers, soluble vascular cell adhesion molecule (sVCAM)-1, and erythrocyte sedimentation rate [ESR]) … while no significant variation was observed in the ‘best available treatment’ group.”

This could eventually lead to a phase out of NSAID use, at least as a treatment for mild-to-moderate osteoarthritis.

Resources:
*  IFT January 11, 2011
* Alternative

Posted By Dr. Mercola | January 31 2011

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Categories
Ailmemts & Remedies

Albinism


Alternative Names
:achromia, achromasia, or achromatosis

Definition:
Albinism  is a congenital disorder characterized by the complete or partial absence of pigment in the skin, hair and eyes due to absence or defect of an enzyme involved in the production of melanin. Albinism results from inheritance of recessive gene alleles and is known to affect all vertebrates, including humans. The most common term used for an organism affected by albinism is “albino”. Additional clinical adjectives sometimes used to refer to animals are “albinoid” and “albinic”.

click & see the pictures

Albinism is associated with a number of vision defects, such as photophobia, nystagmus and astigmatism. Lack of skin pigmentation makes the organism more susceptible to sunburn and skin cancers.

Several different genes are involved in albinism, depending on the specific type of the condition.

Classification in humans:

There are two main categories of albinism in humans:

*In oculocutaneous albinism Types 1-4 with different levels with pigmentation (despite its Latin-derived name meaning “eye-and-skin” albinism), pigment is lacking in the eyes, skin and hair. (The equivalent mutation in non-humans also results in lack of melanin in the fur, scales or feathers.) People with oculocutaneous albinism can have anything from no pigment at all to almost normal levels.

*In ocular albinism, only the eyes lack pigment. People who have ocular albinism have generally normal skin and hair color, although it is typically lighter than either parent. Many even have a normal eye appearance. Also, ocular albinism is generally sex-linked, therefore males are more likely to be affected. Males are without another X chromosome to mask recessive alleles on the X they inherit.

Other conditions include albinism as part of their presentation. These include Hermansky-Pudlak syndrome, Chediak-Higashi syndrome, Griscelli syndrome, Waardenburg syndrome, and Tietz syndrome. These conditions are sometimes classified with albinism. Several have sub-types. Some are easily distinguished by appearance, but in most cases genetic testing is the only way to be certain.

Albinism was formerly categorized as tyrosinase-positive or -negative. In cases of tyrosinase-positive albinism, the enzyme tyrosinase is present. The melanocytes (pigment cells) are unable to produce melanin for any one of a variety of reasons that do not directly involve the tyrosinase enzyme. In tyrosinase-negative cases, either the tyrosinase enzyme is not produced or a nonfunctional version is produced. This classification has been rendered obsolete by recent research.

About one in 17,000 children in the UK is born with some type of albinism.It affects people from all races and its frequency across the human population is estimated to be approximately 1 in 20,000.

Symptoms:
People with albinism are born with little or no pigmentation in their eyes, skin and hair (oculocutaneous albinism) or sometimes in the eyes alone (ocular albinism). But the degree of pigmentation varies (especially in oculocutaneous albinism) and some people gain a little pigmentation in their hair or eyes with age, or develop pigmented freckles on their skin.

Apart from their physical appearance, people with the condition can experience a number of associated problems, depending on which genetic type they have.

Skin

Although the most recognizable form of albinism results in milky white skin, skin pigmentation can range from white to nearly the same as parents or siblings without albinism.

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For some people with albinism, skin pigmentation never changes. For others, melanin production may begin or increase during childhood and adolescence, resulting in slight changes in pigmentation. With exposure to the sun, some people may develop:

*Freckles……CLICK & SEE
*Moles, with or without pigment
*Large freckle-like spots (lentigines)
*The ability to tan

Hair
Hair color can range from very white to brown. People of African or Asian descent who have albinism may have hair color that is yellow, reddish or brown. Hair color may also change by early adulthood.

Eye color
Eye color can range from very light blue to brown and may change with age.

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The lack of pigment in the colored part of your eyes (irises) makes them somewhat translucent. This means that the irises can’t completely block light from entering the eye. Because of this translucence, very light-colored eyes may appear red in some lighting. This occurs because you’re seeing light reflected off the back of the eye and passing back out through the iris again — similar to red eye that occurs in a flash photograph.

Vision
Signs and symptoms of albinism related to eye function include:

*Rapid, involuntary back-and-forth movement of the eyes (nystagmus)
*Inability of both eyes to stay directed at the same point or to move in unison (strabismus)
*Extreme nearsightedness or farsightedness
*Sensitivity to light (photophobia)
*Astigmatism

Causes:
The cause of albinism is a mutation in one of several genes. Each of these genes provides the chemically coded instructions for making one of several proteins involved in the production of melanin. Melanin is produced by cells called melanocytes, which are found in your skin and eyes. A mutation may result in no melanin production at all or a significant decline in the amount of melanin.

In most types of albinism, a person must inherit two copies of a mutated gene — one from each parent — in order to have albinism. If a person has only one copy, then he or she won’t have the disorder.

Impact of mutations on eye development
Regardless of which gene mutation is present, vision impairment is a common characteristic with all types of albinism. These impairments are caused by irregular development of the nerve pathways from the eye to the brain and from abnormal development of the retina.

Types of albinism
The system for classifying types of albinism is based primarily on which mutated gene caused the disorder rather than how it’s manifested. Nonetheless, most types of albinism have some features that distinguish them from each other. Types of albinism include:

*Oculocutaneous albinism.
Oculocutaneous albinism is caused by a mutation in one of four genes. These mutations result in signs and symptoms related to vision (ocular) and those related to skin (cutaneous), hair and iris color.

Oculocutaneous albinism 1 is caused by a mutation in a gene on chromosome 11. Most people with this type of albinism have milky white skin, white hair and blue eyes at birth. Some people with this disorder never experience changes in pigmentation, but others begin to produce melanin during childhood and adolescence. Their hair may become a golden blond or brown. Their skin usually doesn’t change color, but it may tan somewhat. The irises may also change color and lose some of their translucence.

Oculocutaneous albinism 2
is caused by a mutation in a gene on chromosome 15. It’s more common in Sub-Saharan Africans and African-Americans than in other population groups. The hair may be yellow, auburn, ginger or red, the eyes can be blue-gray or tan, and the skin is white at birth. In people of African descent, the skin may be light brown, and in those of Asian or Northern European descent, the skin is usually white. In either case, the skin color is generally close to the family’s coloring, but little bit lighter. With sun exposure, the skin may over time develop freckles, moles or lentigines.
Oculocutaneous albinism 3 (rare cases) is caused by a gene mutation on chromosome 9 and has been primarily identified in black South Africans. People with this disorder usually have reddish-brown skin, ginger or reddish hair, and hazel or brown eyes.

Oculocutaneous albinism 4, caused by a gene mutation on chromosome 5, is a rarer form of the disorder generally presenting signs and symptoms similar to those of type 2. This type of albinism may be one of the most common forms among people of Japanese descent.

*X-linked ocular albinism.
The cause of X-linked ocular albinism, which occurs almost exclusively in males, is a gene mutation on the X chromosome. People who have ocular albinism have the developmental and functional vision problems of albinism. But skin, hair and eye color are generally in the normal range or slightly lighter than that of others in the family.

*Hermansky-Pudlak syndrome. Hermansky-Pudlak syndrome is a rare albinism disorder caused by one of at least seven mutated genes. People with this disorder have signs and symptoms like those of oculocutaneous albinism, but they also develop lung and bowel diseases and a bleeding disorder.

*Chediak-Higashi syndrome. Chediak-Higashi syndrome is a rare form of albinism caused by a mutation in a gene on chromosome 1. Signs and symptoms are also similar to those of oculocutaneous albinism. The hair is usually brown or blond with a silvery sheen, and the skin is usually creamy white to grayish. People with this syndrome have a defect with white blood cells that results in a susceptibility to infections.

Compliccations:
Complications of albinism include physical risks as well as social and emotional challenges.

*In physical terms, humans with albinism commonly have vision problems and need sun protection. But they also face social and cultural challenges (even threats) as the condition is often a source of ridicule, discrimination, or even fear and violence. Cultures around the world have developed many beliefs regarding people with albinism. This folklore ranges from harmless myth to dangerous superstitions that cost human lives. Cultural challenges can be expected to be vastly higher in areas where pale skin and light hair stand out more from the ethnic majority’s average phenotype.

*In African countries such as Tanzania  and Burundi, there has been an unprecedented rise in witchcraft-related killings of albino people in recent years. This is because albino body parts are used in potions sold by witchdoctors. Numerous authenticated incidents have occurred in Africa during the 21st Century. For example, in Tanzania, in September 2009, three men were convicted of killing a 14-year-old albino boy and severing his legs in order to sell them for witchcraft purposes.[19] Again in Tanzania and Burundi in 2010, the murder and dismemberment of a kidnapped albino child is reported from the courts, as part of a continuing problem.

*Other examples: In Zimbabwe, belief that sex with an albinistic woman will cure a man of HIV has led to rapes (and subsequent HIV infection).

*Certain ethnic groups and insular areas exhibit heightened susceptibility to albinism, presumably due to genetic factors (reinforced by cultural traditions). These include notably the Native American Kuna and Zuni nations (respectively of Panama and New Mexico); Japan, in which one particular form of albinism is unusually common; and Ukerewe Island, the population of which shows a very high incidence of albinism.

All of these factors may contribute to social isolation, poor self-esteem and stress.

Treatment :
There’s no cure for albinism, but treatments and aids can help the symptoms and reduce the risk of damage to the skin and eyes.

For the most part, treatment of the eye conditions consists of visual rehabilitation. Surgery is possible on the ocular muscles to decrease nystagmus, strabismus and common refractive errors like astigmatism. Strabismus surgery may improve the appearance of the eyes. Nystagmus-damping surgery can also be performed, to reduce the “shaking” of the eyes back and forth. The effectiveness of all these procedures varies greatly and depends on individual circumstances. More importantly, since surgery will not restore a normal RPE or foveae, surgery will not provide fine binocular vision. In the case of esotropia (the “crossed eyes” form of strabismus), surgery may help vision by expanding the visual field (the area that the eyes can see while looking at one point).

Glasses and other vision aids, large-print materials and CCTV, as well as bright but angled reading lights, can help individuals with albinism, even though their vision cannot be corrected completely. Some people with Albinism do well using bifocals (with a strong reading lens), prescription reading glasses, and/or hand-held devices such as magnifiers or monoculars (a very simple telescope). Contact lenses may be colored to block light transmission through the iris. But in case of nystagmus this is not possible, due to the irritation that is caused by the movement of the eyes. Some use bioptics, glasses which have small telescopes mounted on, in, or behind their regular lenses, so that they can look through either the regular lens or the telescope. Newer designs of bioptics use smaller light-weight lenses. Some US states allow the use of bioptic telescopes for driving motor vehicles.

Although still disputed among the experts, many ophthalmologists recommend the use of spectacles from early childhood onward to allow the eyes the best development possible.

People with Hermansky-Pudlak and Chediak-Higashi syndromes usually require regular specialized care to prevent complications.
Home Remedies & Lifestyle
You can help your child learn self-care practices that should continue into adulthood:

*Use low-vision aids, such as a hand-held magnifying glass, a monocular or a magnifier that attaches to glasses.

*Apply sunscreens with a sun protection factor (SPF) of at least 30 that protects against both UVA and UVB light.

*Avoid high-risk sun exposure, such as being outside in the middle of the day, at high altitudes and on sunny days with thin cloud cover.

*Wear protective clothing, including long-sleeved shirts, long pants and broad-rimmed hats.

*Protect your eyes by wearing dark, UV-blocking sunglasses.

Disclaimer: This information is not meant to be a substitute for professional medical advise or help. It is always best to consult with a Physician about serious health concerns. This information is in no way intended to diagnose or prescribe remedies.This is purely for educational purpose.

Resources:
http://www.bbc.co.uk/health/physical_health/conditions/albinism1.shtml
http://en.wikipedia.org/wiki/Albinism
http://www.mayoclinic.com/health/albinism/DS00941

http://health.howstuffworks.com/skin-care/problems/medical/albinism.htm/printable

http://health.howstuffworks.com/skin-care/problems/medical/albinism2.htm

http://www.makeupbykaty.com/freckles-i-want-more/

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