The prevalence of all forms of albinism varies considerably worldwide has been estimated at approximately 1/ 17, 000 suggesting that about 1 in 70 people carry a gene for oca. oculocutaneous albinism ( oca) is a group of autosomal- recessive conditions characterized by mutations in melanin biosynthesis with resultant absence or reduction of melanin in the melanocytes. herein, we present a rare case of two caucasian sisters diagnosed with oculocutaneous albinism type 1 ( oca1). on physical exam, the tecting the right to life of people living with albinism. a case study of kenya - sylvia waliaula - diploma thesis - albinism law - public law / constitutional law / basic rights - publish your bachelor' s study term paper , master' s thesis, dissertation essay. here we give the case presented by him. case study: a female child aged 4 months was brought to me for hypo pigmentation of skin over whole body hair iris since birth. customer service strengths resume. it was provisionally diagnosed as oculocutaneous albinism. ( type not identified due to lack of laboratory test).
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albinism can affect people of all ethnic backgrounds and has been extensively studied. approximately one in 17, 000 people have one of the types of albinism.
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oculocutaneous albinism ( oca) is a group of inherited disorders of melanin biosynthesis characterized by a generalized reduction in pigmentation of hair, skin and eyes.