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Published on: September 20, 2018
Ocular manifestations of Niemann-Pick disease type B
Margaret M McGovern1, Melissa P Wasserstein, Alan Aron
1Department of Human Genetics and Pediatrics, Mount Sinai School of Medicine, New York, New York 10029, USA. margaret.mcgovern@mssm.edu
Purpose:
To investigate the ocular manifestations in Niemann-Pick disease type B (NPD-B).
Design:
Observational case series.
Participants:
Forty-five patients (23 male and 22 female) with NPD-B from 37 unrelated families.
Methods:
Serial clinical evaluations were carried out over a 2- to 14-year period, including a complete physical examination, neurologic assessment, and ophthalmologic examination. Genotyping of the specific mutations in the acid sphingomyelinase (ASM) gene was performed when possible for genotype-phenotype correlations.
Main Outcome Measures:
Fundus photographs to evaluate the retina, ASM genotype, and neurologic examination findings.
Results:
Ophthalmoscopic examination revealed retinal stigmata in 15 of 45 patients, 3 with macular halos and 12 with cherry red maculae. Neurologic examinations did not reveal any evidence of neurodegeneration, and there was no consistent relationship between retinal findings and genotype.
Conclusions:
The presence of macular halos and/or cherry red maculae is not an absolute predictor of neurodegeneration, but should prompt a thorough evaluation to determine the underlying etiology and the precise diagnosis.
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