Literature DB >> 2779741

Autosomal recessive microcephaly, mental retardation with nonpigmentary retinopathy and a distinctive electroretinogram.

M G Harbord1, S R Lambert, A Kriss, E M Brett, M Baraitser, G Supramaniam.   

Abstract

The association of microcephaly and mental retardation with a non-pigmentary retinopathy is described in three siblings of consanguineous parents. The electroretinogram showed the distinctive appearance of markedly attenuated "b" wave but normal "a" wave suggestive of a retinal dystrophy primarily affecting post-receptoral elements in the inner retina. This appears to be an autosomal recessive condition which has not been previously reported.

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Year:  1989        PMID: 2779741     DOI: 10.1055/s-2008-1071279

Source DB:  PubMed          Journal:  Neuropediatrics        ISSN: 0174-304X            Impact factor:   1.947


  1 in total

1.  Electrophysiologic evaluation of the visual pathway in children. Case reports.

Authors:  J Brecelj; B Stirn-Kranjc
Journal:  Doc Ophthalmol       Date:  1992       Impact factor: 2.379

  1 in total

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