1. vicky s. wang

2. no color  Albinism is a defect of melanin production that results in little or no color (pigment) in the skin, hair, and eyes.  Melanin is a skin pigment (substance that gives the skin its color). Dark- skinned people have more melanin than light- skinned people. Melanin comes in two types: pheomelanin (red) and eumelanin (very dark brown). Both amount and type are determined by four to six genes which operate under incomplete dominancepheomelanineumelanin  Melanin pigment 

3.  A person with albinism will have one of the following symptoms :  Absence of color  Absence of color in the hair, skin, or iris of the eye  Lighter-than-normal skin and hair  Patchy, missing skin color  Albino bunny! 

5. white negro  A man in the 17th century named Balthazar Telez, who was an explorer, came up with the name "Albino", which means white negro, after he saw an albino African tribe. Balthazar thought he was seeing two different races of people. This was the first discovery of albinism.  The first ever reported case of albinism that scientifically came up was in the year 1908. Most of the individuals that have suffered from albinism have a long history of being ostracized and rebuked by society.

6.  Oculocutaneous  involves dilution of the color of the hair, skin and eyes  most common form of albinism  Ocular  melanin pigment mainly missing from the eyes while the skin and hair appear normal or only slightly lighter  accounts for 10-15% of all albinism cases

7.  There are two main types of Oculocutaneous albinism:  Type 1 albinism is caused by defects that affect production of the pigment, melanin.  Type 2 albinism is due to a defect in the “P gene”. People with this type have slight coloring at birth.  The most severe form of albinism is called oculocutaneous albinism. People with this type of albinism have white or pink hair, skin, and iris color, as well as vision problems.

8.  Is cause by genetic defect of the tyrosinase enzyme that helps the body to change the amino acid tyrosine into melanin pigment  OA1 Gene Mutations Associated with Ocular Albinism type 1

9.  Oculocutaneous albinism type 2 (OCA2) is an recessive disorder characterized by defective melanin production of the skin, hair, and eyes, which is caused by mutations of the "P" gene. "P" gene  The specific function of P has not been clarified, although it is likely to act as a transporter in the melanosomal membrane.  a melanosome is an organelle containing melanin

10. OCULOCUTANEOUS OCULAR

11.  Both are inherited in a autosomal recessive manner  About 1 in 70 people have a gene for albinism. Couples whom are each carriers of the recessive albinism gene have a 1 in 4 chance of producing a child with albinism.

12.  Skin problems  Easily sunburn  Increased chance of getting skin cancers  Eye problems  Impaired vision: although not blind, vision is impaired and may not be fully corrected with glasses. Varying degrees of near- sightedness or far-sightedness exist.  Photophobia: sensitivity to light or glare  Nystagmus: involuntary movement of the eyes back and forth  Strabismus: eyes do not fixate and track together  Retinal involvement: this is an important area of the eye as it is responsible for sending signals to the brain. Impaired transmission of signals causes various vision disorders

13.  Albinism can be diagnosed by observation of major or total absence of pigmentation of the appearance of the skin, hair, and eyes.  The most accurate way to determine albinism and its specific type is genetic testing. This is helpful in families with albinism and is useful for specific, isolated populations who carry the trait in them.  Recently, a blood test has been developed that can identify carriers of the gene for some types of albinism.  There is no cure for albinism. Treatment is aimed to ease the symptoms and it depends on the extent of the disorder. Treatment of the eye conditions consists of visual rehabilitation.

15.  Albinism. 15 6 2009. 25 3 2010.  definition of melanin. 3 26 1998. 24 3 2010.  Fawn, Mike. Albinism- A History of Albinism. 25 3 2010.  Saitoh, Shinji. Oculocutaneous albinism type 2 with a P gene missense mutation in a patient with Angelman syndrome. 25 3 2010.