Literature DB >> 15200506

Three new families with X-linked mental retardation caused by the 428-451dup(24bp) mutation in ARX.

M W Partington1, G Turner, J Boyle, J Gécz.   

Abstract

Three families with X-linked mental retardation caused by a 24 base-pair duplication in ARX[428-451dup(24 bp)] are reported. The clinical features in these and six other published families are reviewed. In general, the clinical picture is variable. Mental retardation ranges from mild to severe. Infantile spasms (West syndrome) occurred in 12.5% and other less severe forms of seizures in 37.5%. Characteristic dystonic movements of the hands were seen in 63% and dysarthria in 54%. The focal dystonia, in association with mental retardation, may prove to be diagnostic of this mutation.

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Year:  2004        PMID: 15200506     DOI: 10.1111/j.0009-9163.2004.00268.x

Source DB:  PubMed          Journal:  Clin Genet        ISSN: 0009-9163            Impact factor:   4.438


  19 in total

1.  Screening of ARX in mental retardation families: Consequences for the strategy of molecular diagnosis.

Authors:  K Poirier; D Lacombe; B Gilbert-Dussardier; M Raynaud; V Desportes; A P M de Brouwer; C Moraine; J P Fryns; H H Ropers; C Beldjord; J Chelly; T Bienvenu
Journal:  Neurogenetics       Date:  2005-10-19       Impact factor: 2.660

Review 2.  Genetics, molecular biology, and phenotypes of x-linked epilepsy.

Authors:  Hao Deng; Wen Zheng; Zhi Song
Journal:  Mol Neurobiol       Date:  2013-11-22       Impact factor: 5.590

3.  Mutations in the RSK2(RPS6KA3) gene cause Coffin-Lowry syndrome and nonsyndromic X-linked mental retardation.

Authors:  M Field; P Tarpey; J Boyle; S Edkins; J Goodship; Y Luo; J Moon; J Teague; M R Stratton; P A Futreal; R Wooster; F L Raymond; G Turner
Journal:  Clin Genet       Date:  2006-12       Impact factor: 4.438

4.  Low amounts of PHOX2B expanded alleles in asymptomatic parents suggest unsuspected recurrence risk in congenital central hypoventilation syndrome.

Authors:  Tiziana Bachetti; Sara Parodi; Marco Di Duca; Giuseppe Santamaria; Roberto Ravazzolo; Isabella Ceccherini
Journal:  J Mol Med (Berl)       Date:  2011-02-19       Impact factor: 4.599

5.  Mutations of CDKL5 cause a severe neurodevelopmental disorder with infantile spasms and mental retardation.

Authors:  Linda S Weaving; John Christodoulou; Sarah L Williamson; Kathie L Friend; Olivia L D McKenzie; Hayley Archer; Julie Evans; Angus Clarke; Gregory J Pelka; Patrick P L Tam; Catherine Watson; Hooshang Lahooti; Carolyn J Ellaway; Bruce Bennetts; Helen Leonard; Jozef Gécz
Journal:  Am J Hum Genet       Date:  2004-10-18       Impact factor: 11.025

6.  Is there a Mendelian transmission ratio distortion of the c.429_452dup(24bp) polyalanine tract ARX mutation?

Authors:  Cheryl Shoubridge; Alison Gardner; Charles E Schwartz; Anna Hackett; Michael Field; Jozef Gecz
Journal:  Eur J Hum Genet       Date:  2012-04-11       Impact factor: 4.246

7.  CDKL5 and ARX mutations in males with early-onset epilepsy.

Authors:  Ghayda M Mirzaa; Alex R Paciorkowski; Eric D Marsh; Elizabeth M Berry-Kravis; Livija Medne; Asem Alkhateeb; Art Grix; Elaine C Wirrell; Berkley R Powell; Katherine C Nickels; Barbara Burton; Andrea Paras; Katherine Kim; Wendy Chung; William B Dobyns; Soma Das
Journal:  Pediatr Neurol       Date:  2013-05       Impact factor: 3.372

8.  Mutations in the nuclear localization sequence of the Aristaless related homeobox; sequestration of mutant ARX with IPO13 disrupts normal subcellular distribution of the transcription factor and retards cell division.

Authors:  Cheryl Shoubridge; May Huey Tan; Tod Fullston; Desiree Cloosterman; David Coman; George McGillivray; Grazia M Mancini; Tjitske Kleefstra; Jozef Gécz
Journal:  Pathogenetics       Date:  2010-01-05

9.  Mutations in ARX Result in Several Defects Involving GABAergic Neurons.

Authors:  Gaëlle Friocourt; John G Parnavelas
Journal:  Front Cell Neurosci       Date:  2010-03-11       Impact factor: 5.505

10.  Copy number variants in patients with intellectual disability affect the regulation of ARX transcription factor gene.

Authors:  Minaka Ishibashi; Elizabeth Manning; Cheryl Shoubridge; Monika Krecsmarik; Thomas A Hawkins; Jean Giacomotto; Ting Zhao; Thomas Mueller; Patricia I Bader; Sau W Cheung; Pawel Stankiewicz; Nicole L Bain; Anna Hackett; Chilamakuri C S Reddy; Alejandro S Mechaly; Bernard Peers; Stephen W Wilson; Boris Lenhard; Laure Bally-Cuif; Jozef Gecz; Thomas S Becker; Silke Rinkwitz
Journal:  Hum Genet       Date:  2015-09-04       Impact factor: 4.132

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