Oculocutaneous albinism: A group of inherited disorders characterized by varying degrees of lack of pigmentation in the skin, eyes and hair. More detailed information about the symptoms, causes, and treatments of Oculocutaneous albinism is available below.
See full list of 9 symptoms of Oculocutaneous albinism
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Read more about Deaths and Oculocutaneous albinism.
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Read more about causes of Oculocutaneous albinism.
Research the causes of these diseases that are similar to, or related to, Oculocutaneous albinism:
Commonly undiagnosed diseases in related medical categories:
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Read more about Misdiagnosis and Oculocutaneous albinism
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Medical research articles related to Oculocutaneous albinism include:
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The US based website ClinicalTrials.gov lists information on both federally and privately supported clinical trials using human volunteers.
Some of the clinical trials listed on ClinicalTrials.gov for Oculocutaneous albinism include:
Read more about Clinical Trials for Oculocutaneous albinism
Types of Oculocutaneous albinism
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Ophanet, a consortium of European partners,
currently defines a condition rare when it affects 1 person per 2,000.
They list Oculocutaneous albinism as a "rare disease".
Source - Orphanet
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