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Minimal pigment oculocutaneous albinism type 1

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Name:
Minimal pigment oculocutaneous albinism type 1
Description:
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.
ORPHAcode:
352734
Synonyms:
MP OCA type 1
OCA1-MP
XREF(s):
Orphanet
ICD-10
Analyte(s):
TYR
Created:
13 May 2019 - 01:02
Changed:
22 Jun 2023 - 16:14
  • Ocular and oculocutaneous albinism - UGent
    Gene % of coding sequence sufficiently covered to detect heterozygous mutations Copy number variation Comments
    TYR 100.00 1
    OCA2 100.00 1
    TYRP1 100.00 0
    SLC45A2 100.00 0
    SLC24A5 100.00 0
    LRMDA 100.00 0
    GPR143 100.00 1
    DCT 100.00 0