Literature DB >> 15216544

Perrault syndrome: evidence for progressive nervous system involvement.

Agata Fiumara1, Giovanni Sorge, Antonio Toscano, Enrico Parano, Lorenzo Pavone, John M Opitz.   

Abstract

Perrault syndrome (PS) comprises gonadal dysgenesis and sensorineural deafness in females, and deafness in affected males. More recent studies have asked whether the neurological signs in some of the patients are a coincidental finding or part of the syndrome. We report on two pairs of sisters with gonadal dysgenesis and deafness, cerebral, and ocular involvement who developed a progressive, severe sensory, and motor neuropathy. This observation constitutes further evidence of peripheral nervous system involvement in PS. Based on the clinical observations of known patients, two forms of PS may be distinguished: one apparently non-progressive form and another (exemplified by our two sets of sisters) with apparently progressive axonal-cerebellar degeneration. Copyright 2004 Wiley-Liss, Inc.

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Year:  2004        PMID: 15216544     DOI: 10.1002/ajmg.a.20616

Source DB:  PubMed          Journal:  Am J Med Genet A        ISSN: 1552-4825            Impact factor:   2.802


  21 in total

1.  Perrault syndrome: further evidence for genetic heterogeneity.

Authors:  Emma M Jenkinson; Jill Clayton-Smith; Sarju Mehta; Christopher Bennett; Willie Reardon; Andrew Green; Simon H S Pearce; Giuseppe De Michele; Gerard S Conway; Deirdre Cilliers; Natalie Moreton; Julian R E Davis; Dorothy Trump; William G Newman
Journal:  J Neurol       Date:  2011-10-27       Impact factor: 4.849

2.  Mutations in the DBP-deficiency protein HSD17B4 cause ovarian dysgenesis, hearing loss, and ataxia of Perrault Syndrome.

Authors:  Sarah B Pierce; Tom Walsh; Karen M Chisholm; Ming K Lee; Anne M Thornton; Agata Fiumara; John M Opitz; Ephrat Levy-Lahad; Rachel E Klevit; Mary-Claire King
Journal:  Am J Hum Genet       Date:  2010-07-30       Impact factor: 11.025

3.  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

4.  Genetic pathogenesis of Perrault Syndrome.

Authors:  Esma Sarıkaya
Journal:  J Turk Ger Gynecol Assoc       Date:  2012-06-01

5.  Mutations in mitochondrial histidyl tRNA synthetase HARS2 cause ovarian dysgenesis and sensorineural hearing loss of Perrault syndrome.

Authors:  Sarah B Pierce; Karen M Chisholm; Eric D Lynch; Ming K Lee; Tom Walsh; John M Opitz; Weiqing Li; Rachel E Klevit; Mary-Claire King
Journal:  Proc Natl Acad Sci U S A       Date:  2011-04-04       Impact factor: 11.205

6.  Mutations in Twinkle primase-helicase cause Perrault syndrome with neurologic features.

Authors:  Hiroyuki Morino; Sarah B Pierce; Yukiko Matsuda; Tom Walsh; Ryosuke Ohsawa; Marta Newby; Keiko Hiraki-Kamon; Masahito Kuramochi; Ming K Lee; Rachel E Klevit; Alan Martin; Hirofumi Maruyama; Mary-Claire King; Hideshi Kawakami
Journal:  Neurology       Date:  2014-10-29       Impact factor: 9.910

7.  Perrault syndrome - a rare case report.

Authors:  Geethalakshmi Sampathkumar; Narendrakumar Veerasigamani
Journal:  J Clin Diagn Res       Date:  2015-03-01

Review 8.  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

Review 9.  Unresolved questions regarding human hereditary deafness.

Authors:  A U Rehman; T B Friedman; A J Griffith
Journal:  Oral Dis       Date:  2016-07-11       Impact factor: 3.511

10.  Mutations of SGO2 and CLDN14 collectively cause coincidental Perrault syndrome.

Authors:  R Faridi; A U Rehman; R J Morell; P L Friedman; L Demain; S Zahra; A A Khan; D Tohlob; M Z Assir; G Beaman; S N Khan; W G Newman; S Riazuddin; T B Friedman
Journal:  Clin Genet       Date:  2016-11-16       Impact factor: 4.438

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