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Article

Oculocutaneous albinism type 1A: a case report.

Dermatology online journal - 15 Nov 2008

Karaman Ali

Abstract excerpt

The term, oculocutaneous albinism (OCA), describes a group of inherited disorders of melanin biosynthesis that exhibits congenital hypopigmentation of ocular and cutaneous tissues. The clinical spectrum of OCA ranges from a complete lack of melanin pigmentation to mildly hypopigmented forms. OCA1A is the most severe type with a complete lack of melanin production throughout life; the milder forms OCA1B, OCA2,...

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Source

Identifiers

PMID: 19094851

Genes

OCA2
TYR
TYRP1

Provenance

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Source receipt: pubmed, retrieved 7 Sept 2026.

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