Literature DB >> 3917610

Ocular findings in a new heritable syndrome of brain, eye, and urogenital abnormalities.

J S Duker, J S Weiss, M Siber, F R Bieber, D M Albert.   

Abstract

We studied the clinical and histopathologic ocular findings in four related males with a newly recognized syndrome consisting of microphthalmos, microencephaly, mental retardation, agenesis of the corpus callosum, hypospadius, and cryptorchidism with X-linked recessive inheritance. The ocular abnormalities include microphthalmos, corneal pannus and hypoplasia, cataracts, uveal hypoplasia, retinal dysplasia, optic nerve hypoplasia, and congenital blepharoptosis. In case 4, a female twin who died in utero (at 15 weeks' gestation) showed none of the ocular abnormalities.

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Year:  1985        PMID: 3917610     DOI: 10.1016/s0002-9394(14)75866-0

Source DB:  PubMed          Journal:  Am J Ophthalmol        ISSN: 0002-9394            Impact factor:   5.258


  3 in total

1.  Mapping the gene for X-linked cataracts and microcornea with facial, dental, and skeletal features to Xp22: an appraisal of the Nance-Horan syndrome.

Authors:  R A Lewis
Journal:  Trans Am Ophthalmol Soc       Date:  1989

2.  Ocular malformations and lissencephaly.

Authors:  M Warburg
Journal:  Eur J Pediatr       Date:  1987-09       Impact factor: 3.183

3.  Microcephaly, microphthalmos, and retinal folds: report of a family.

Authors:  I D Young; A R Fielder; K Simpson
Journal:  J Med Genet       Date:  1987-03       Impact factor: 6.318

  3 in total

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