Literature DB >> 8923934

Neurologic anomalies of Perrault syndrome.

M E Gottschalk1, S B Coker, L A Fox.   

Abstract

We report on an 18-year-old man with neurosensory hearing loss and his sister with neurosensory hearing loss, ovarian dysgenesis, mental retardation, generalized ataxia of the trunk and limbs, and saccadic dysmetria. A CT scan showed cerebellar hypoplasia. The cardinal manifestations of Perrault syndrome in females are neurosensory hearing loss and ovarian dysgenesis. Other anomalies, including neurologic and skeletal, have been reported in other individuals with Perrault syndrome. We review the neurologic anomalies in previous patients with Perrault syndrome. Neurologic data are available on 14 of 21 girls; 7 of 14 had neurologic abnormalities. The high incidence of neurologic anomalies suggest that ataxia or mental retardation may not be just coincidental findings, but pleiotropic manifestations of Perrault syndrome.

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Year:  1996        PMID: 8923934     DOI: 10.1002/(SICI)1096-8628(19961111)65:4<274::AID-AJMG5>3.0.CO;2-P

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


  14 in total

1.  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

2.  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

3.  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

Review 4.  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

5.  A rare cause for primary amenorrhoea.

Authors:  Kaderthambi Hajamohideen Noorul Ameen; Rakesh Pinninti
Journal:  J Hum Reprod Sci       Date:  2012-05

6.  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

Review 7.  New insights into the genetic basis of infertility.

Authors:  Thejaswini Venkatesh; Padmanaban S Suresh; Rie Tsutsumi
Journal:  Appl Clin Genet       Date:  2014-12-01

8.  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

Review 9.  New insights into Perrault syndrome, a clinically and genetically heterogeneous disorder.

Authors:  Rabia Faridi; Alessandro Rea; Cristina Fenollar-Ferrer; Raymond T O'Keefe; Shoujun Gu; Zunaira Munir; Asma Ali Khan; Sheikh Riazuddin; Michael Hoa; Sadaf Naz; William G Newman; Thomas B Friedman
Journal:  Hum Genet       Date:  2021-08-02       Impact factor: 4.132

10.  A rare cause for primary amenorrhea: Sporadic perrault syndrome.

Authors:  K H Noorul Ameen; Rakesh Pinninti
Journal:  Indian J Endocrinol Metab       Date:  2012-09
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