Artigo Revisado por pares

Chediak-Nigashi Syndrome: Ocular Findings

1980; Slack Incorporated (United States); Volume: 17; Issue: 2 Linguagem: Inglês

10.3928/0191-3913-19800301-04

ISSN

1938-2405

Autores

David BenEzra, Fekede Mengistu, Gabriel Cividalli, Zvi Weizman, Saul Merin, E. Auerbach,

Tópico(s)

Autoimmune and Inflammatory Disorders Research

Resumo

A case of Chediak-Higashi syndrome diagnosed by its characteristic ocular findings is described. The appearance of the optic disc and the contrast between total (or nearly total) lack of pigment in the pigment epithelium and the relatively unaffected choroidal pigmentation are believed to be observations of paramount importance in the differential diagnosis by ophthalmoscopic examination. Electrophysiological tests of our case showed abnormal responses and a further deterioration of the ERG and VEP on repeated examinations. Electron microscopic study of a conjunctival biopsy revealed the presence of pathognomonic giant intracytoplasmic lysosomal granules in stromal fibroblasts and, thus, can be used as an adjunct test in suspected cases of Chediak-Higashi syndrome.

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