Diagnosis of oculocutaneous albinism with molecular analysis

C. G. Summers, W. S. Oetting, R. A. King

Research output: Contribution to journalArticlepeer-review

15 Scopus citations


PURPOSE: To use molecular analysis to diagnose oculocutaneous albinism in a patient with an atypical clinical presentation. METHODS: A 34-year-old woman with a history of strabismus and absent cutaneous pigment underwent comprehensive ophthalmic examination, visual-evoked potentials to detect altered optic decussation, and molecular analysis. RESULTS: Examination showed fine nystagmus, iris transillumination, foveal hypoplasia, and corrected visual acuity of 20/25 in each eye. Misrouting of the retinostriate fibers was demonstrated with visual-evoked potentials. Mutations in the tyrosinase gene established the diagnosis of oculocutaneous albinism 1 even though the patient had atypical clinical features. CONCLUSION: Molecular analysis can establish the diagnosis of oculocutaneous albinism 1 in the patient with atypical ocular features.

Original languageEnglish (US)
Pages (from-to)724-726
Number of pages3
JournalAmerican journal of ophthalmology
Issue number6
StatePublished - 1996

Bibliographical note

Funding Information:
Department of Ophthalmology, University of Minnesota. Supported by an unrestricted grant from Research to Prevent Blindness, inc., New York, New York.

Copyright 2017 Elsevier B.V., All rights reserved.


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