Literature DB >> 8030674

Deafness, sensory neuropathy, and ovarian dysgenesis: a new syndrome or a broader spectrum of Perrault syndrome?

W H Linssen1, M J Van den Bent, H G Brunner, P J Poels.   

Abstract

We report on 3 sibs (2 males and one female) with sensorineural deafness. The presence of ovarian dysgenesis in the girl suggested a diagnosis of Perrault syndrome. In addition our patients have a sensory polyneuropathy and amelogenesis imperfecta. Two of the patients have mild mental retardation, fine choreatic movements, and dyspraxia. It is discussed whether these findings are part of a separate clinical entity or should be included within the spectrum of the Perrault syndrome.

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Year:  1994        PMID: 8030674     DOI: 10.1002/ajmg.1320510117

Source DB:  PubMed          Journal:  Am J Med Genet        ISSN: 0148-7299


  6 in total

1.  Perrault syndrome is caused by recessive mutations in CLPP, encoding a mitochondrial ATP-dependent chambered protease.

Authors:  Emma M Jenkinson; Atteeq U Rehman; Tom Walsh; Jill Clayton-Smith; Kwanghyuk Lee; Robert J Morell; Meghan C Drummond; Shaheen N Khan; Muhammad Asif Naeem; Bushra Rauf; Neil Billington; Julie M Schultz; Jill E Urquhart; Ming K Lee; Andrew Berry; Neil A Hanley; Sarju Mehta; Deirdre Cilliers; Peter E Clayton; Helen Kingston; Miriam J Smith; Thomas T Warner; Graeme C Black; Dorothy Trump; Julian R E Davis; Wasim Ahmad; Suzanne M Leal; Sheikh Riazuddin; Mary-Claire King; Thomas B Friedman; William G Newman
Journal:  Am J Hum Genet       Date:  2013-03-28       Impact factor: 11.025

Review 2.  Mitochondrial Quality Control Proteases in Neuronal Welfare.

Authors:  Roman M Levytskyy; Edward M Germany; Oleh Khalimonchuk
Journal:  J Neuroimmune Pharmacol       Date:  2016-05-02       Impact factor: 4.147

3.  Hypergonadotropic hypogonadism, progressive early-onset spinocerebellar ataxia, and late-onset sensorineural hearing loss: case report and literature review.

Authors:  E Sarikaya; Cg Ensert; Hc Gulerman
Journal:  Balkan J Med Genet       Date:  2011-12       Impact factor: 0.519

4.  A homozygous missense variant in HSD17B4 identified in a consanguineous Chinese Han family with type II Perrault syndrome.

Authors:  Kui Chen; Ke Yang; Su-Shan Luo; Chen Chen; Ying Wang; Yi-Xuan Wang; Da-Ke Li; Yu-Jie Yang; Yi-Lin Tang; Feng-Tao Liu; Jian Wang; Jian-Jun Wu; Yi-Min Sun
Journal:  BMC Med Genet       Date:  2017-08-23       Impact factor: 2.103

5.  Loss of mitochondrial peptidase Clpp leads to infertility, hearing loss plus growth retardation via accumulation of CLPX, mtDNA and inflammatory factors.

Authors:  Suzana Gispert; Dajana Parganlija; Michael Klinkenberg; Stefan Dröse; Ilka Wittig; Michel Mittelbronn; Pawel Grzmil; Sebastian Koob; Andrea Hamann; Michael Walter; Finja Büchel; Thure Adler; Martin Hrabé de Angelis; Dirk H Busch; Andreas Zell; Andreas S Reichert; Ulrich Brandt; Heinz D Osiewacz; Marina Jendrach; Georg Auburger
Journal:  Hum Mol Genet       Date:  2013-07-12       Impact factor: 6.150

6.  Kohlschütter-Tönz syndrome: mutations in ROGDI and evidence of genetic heterogeneity.

Authors:  Arianna Tucci; Eleanna Kara; Anna Schossig; Nicole I Wolf; Vincent Plagnol; Katherine Fawcett; Coro Paisán-Ruiz; Matthew Moore; Dena Hernandez; Sebastiano Musumeci; Michael Tennison; Raoul Hennekam; Silvia Palmeri; Alessandro Malandrini; Salmo Raskin; Dian Donnai; Corina Hennig; Andreas Tzschach; Roel Hordijk; Thomas Bast; Katharina Wimmer; Chien-Ning Lo; Simon Shorvon; Heather Mefford; Evan E Eichler; Roger Hall; Ian Hayes; John Hardy; Andrew Singleton; Johannes Zschocke; Henry Houlden
Journal:  Hum Mutat       Date:  2012-11-27       Impact factor: 4.878

  6 in total

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