Minimal pigment oculocutaneous albinism type 1

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Minimal pigment oculocutaneous albinism type 1

Synonyms: MP OCA type 1 | OCA1-MP

An extremely rare form of Oculocutaneous albinism type 1 with minimal pigment present characterized by blond hair (white at birth) variable iris transillumination (blue irides at birth followed by minimal development of pigment during the first decade of life) visual acuity ranging from 20/80-20/200 and white skin with or without skin nevi.

Data from Orphanet are used to provide information on a disease's name, synonym(s), and overview.

Reference: Access aggregated data from Orphanet at Orphadata.

Orphadata: Free access data from Orphanet. © INSERM 1999. Available on http: // Data version September 2023.

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Minimal pigment oculocutaneous albinism type 1?

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Advocacy Organizations

Mississippi Metabolics Foundation

Mississippi Metabolics Foundation (MMF) was founded to raise awareness, educate, and provide support to those living or caring for someone with genetic metabolic disorders/inborn errors of metabolism (IEM).

Clinical Trials

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