Kubal Anup, Dagnelie Gislin, Goldberg Morton
Wilmer Eye Institute, Johns Hopkins School of Medicine, 600 N.Wolfe Street, Baltimore, MD 21287, USA.
J AAPOS. 2009 Dec;13(6):610-2. doi: 10.1016/j.jaapos.2009.09.015.
A 9-year-old Caucasian girl of northern European ancestry presented with findings suggestive of ocular albinism, although she maintains good visual acuity and lacks nystagmus and photophobia. DNA analysis revealed that the patient is a compound heterozygote for mutations in the tyrosinase gene, which is typically associated with overt, generalized oculocutaneous albinism and severe ocular symptoms. Her particular genotype confers no apparent cutaneous disease and only mild ocular features.
