Retinitis pigmentosa.

Abstract:

:Retinitis pigmentosa is a clinically and genetically heterogeneous group of hereditary disorders in which there is progressive loss of photoreceptor and pigment epithelial function. The prevalence of retinitis pigmentosa is between 1/3000 and 1/5000 making it one of the most common causes of visual impairment in all age groups. The natural history, differential diagnosis, diagnostic clinical and electrophysiologic findings are reviewed. Generalization about the different genetic subtypes of retinitis pigmentosa are reviewed along with the uses of DNA probes for linkage studies. Syndromes in which retinitis pigmentosa is a manifestation are summarized.

journal_name

Surv Ophthalmol

journal_title

Survey of ophthalmology

authors

Pagon RA

doi

10.1016/0039-6257(88)90085-9

subject

Has Abstract

pub_date

1988-11-01 00:00:00

pages

137-77

issue

3

eissn

0039-6257

issn

1879-3304

pii

0039-6257(88)90085-9

journal_volume

33

pub_type

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