A patient with subclinical oculocutaneous albinism type 2 diagnosed on getting severely sunburned

Dermatology. 2005;210(4):322-3. doi: 10.1159/000084758.

Abstract

P-gene-related oculocutaneous albinism (OCA2) is an autosomal recessive disorder. The phenotype is typically somewhat less severe than that of the tyrosinase-negative type (OCA1A). One of the mutations in the P gene, A481T, is associated with a mild phenotype, occasionally with no distinctive skin manifestations, which is called subclinical OCA. We present a Japanese patient having the A481T mutant allele in the P gene with subclinical oculocutaneous albinism diagnosed on getting severely sunburned. The A481T mutant allele is relatively common in the Caucasian population as well as in Japan, indicating that a number of subclinical patients of OCA2 might exist not only in Japan, but also all over the world.

Publication types

  • Case Reports
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Albinism, Oculocutaneous / complications
  • Albinism, Oculocutaneous / diagnosis
  • Albinism, Oculocutaneous / genetics*
  • Alleles
  • DNA Mutational Analysis
  • Follow-Up Studies
  • Genetic Predisposition to Disease*
  • Humans
  • Japan
  • Male
  • Membrane Transport Proteins / genetics*
  • Mutation*
  • Risk Assessment
  • Severity of Illness Index
  • Sunburn / complications
  • Sunburn / diagnosis
  • Sunburn / genetics*

Substances

  • Membrane Transport Proteins
  • OCA2 protein, human