Albinism overview: Difference between revisions
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==Overview== | ==Overview== | ||
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==Diagnosis== | ==Diagnosis== | ||
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===Secondary Prevention=== | ===Secondary Prevention=== | ||
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Revision as of 12:42, 21 July 2016
Albinism Microchapters |
Diagnosis |
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Treatment |
Case Studies |
Albinism overview On the Web |
American Roentgen Ray Society Images of Albinism overview |
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief:
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Overview
Albinism (from Latin albus; extended etymology), more technically hypomelanism or hypomelanosis, is a form of hypopigmentary congenital disorder, characterized by a lack of melanin pigment in the eyes, skin and hair (or more rarely the eyes alone). Albinism results from inheritance of recessive genes. The condition is known to affect mammals, fish, birds, reptiles, and amphibians. While the most common term for an organism affected by albinism is "albino" (noun and adjective), the word is sometimes used in a derogatory way towards people; more neutral terms are "albinistic" (adjective) and "person with albinism" (noun). Additional clinical adjectives sometimes used to refer to animals are "albinoid" and "albinic".