Literature DB >> 6837691

Carrier detection in tapetoretinal degeneration in association with medullary cystic disease.

B C Polak, F H van Lith, J W Delleman, A T van Balen.   

Abstract

We conducted electro-oculographic and electroretinographic studies of six families with the autosomal recessively inherited Senior-Loken syndrome (juvenile familial nephronophthisis or medullary cystic disease in association with tapetoretinal degeneration). Sixteen patients had both renal and ocular involvement. In two families consanguinity between the patients was established. Routine ophthalmologic examination of relatives without renal involvement showed no retinal abnormalities, but electro-oculographic and electroretinographic studies were helpful in detecting 16 asymptomatic family members who carried the gene.

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Year:  1983        PMID: 6837691     DOI: 10.1016/0002-9394(83)90269-6

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


  5 in total

1.  Electrophysiological findings of neuronal ceroid lipofuscinosis in heterozygotes.

Authors:  I Gottlob; K P Leipert; A Kohlschütter; H H Goebel
Journal:  Graefes Arch Clin Exp Ophthalmol       Date:  1988       Impact factor: 3.117

2.  Mapping of gene loci for nephronophthisis type 4 and Senior-Løken syndrome, to chromosome 1p36.

Authors:  Maria J Schuermann; Edgar Otto; Achim Becker; Katrin Saar; Franz Rüschendorf; Bettine C Polak; Sirpa Ala-Mello; Julia Hoefele; Alexander Wiedensohler; Maria Haller; Heymut Omran; Peter Nürnberg; Friedhelm Hildebrandt
Journal:  Am J Hum Genet       Date:  2002-03-27       Impact factor: 11.025

Review 3.  Aplasia of the cerebellar vermis associated with chronic renal disease. A report of six cases and a review of the literature.

Authors:  B Keuth; U Alon; A Fuchshuber; D Michalk; U Querfeld
Journal:  Eur J Pediatr       Date:  1996-11       Impact factor: 3.183

4.  A gene mutated in nephronophthisis and retinitis pigmentosa encodes a novel protein, nephroretinin, conserved in evolution.

Authors:  Edgar Otto; Julia Hoefele; Rainer Ruf; Adelheid M Mueller; Karl S Hiller; Matthias T F Wolf; Maria J Schuermann; Achim Becker; Ralf Birkenhäger; Ralf Sudbrak; Hans C Hennies; Peter Nürnberg; Friedhelm Hildebrandt
Journal:  Am J Hum Genet       Date:  2002-08-29       Impact factor: 11.025

Review 5.  The nephronophthisis complex: clinical and genetic aspects.

Authors:  F Hildebrandt; R Waldherr; R Kutt; M Brandis
Journal:  Clin Investig       Date:  1992-09
  5 in total

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