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Oculocutaneous albinism

Oculocutaneous albinism (OCA) describes a group of inherited disorders of melanin biosynthesis characterized by a generalized reduction in pigmentation of hair, skin and eyes and variable ocular findings including nystagmus, reduced visual acuity and photophobia. Variants include OCA1A (the most severe form), OCA1B, OCA1-minimal pigment (OCA1-MP), OCA1-temperature sensitive (OCA1-TS), OCA2, OCA3, OCA4, OCA5, OCA6 and OCA7.

4 trials tagged with this condition →

Oculocutaneous albinism type 1 0 trials · 1 incl. sub-types Sub-types →
Autosomal dominant oculocutaneous albinism 0 trials
Oculocutaneous albinism type 2 0 trials
Oculocutaneous albinism type 3 0 trials
Oculocutaneous albinism type 4 0 trials
Oculocutaneous albinism type 5 0 trials
Oculocutaneous albinism type 6 0 trials
Oculocutaneous albinism type 7 0 trials
Oculocutaneous albinism type 8 0 trials