Literature DB >> 10521307

A new neurological syndrome with mental retardation, choreoathetosis, and abnormal behavior maps to chromosome Xp11.

E Reyniers1, P Van Bogaert, N Peeters, L Vits, F Pauly, E Fransen, N Van Regemorter, R F Kooy.   

Abstract

Choreoathetosis is a major clinical feature in only a small number of hereditary neurological disorders. We define a new X-linked syndrome with a unique clinical picture characterized by mild mental retardation, choreoathetosis, and abnormal behavior. We mapped the disease in a four-generation pedigree to chromosome Xp11 by linkage analysis and defined a candidate region containing a number of genes possibly involved in neuronal signaling, including a potassium channel gene and a neuronal G protein-coupled receptor.

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Year:  1999        PMID: 10521307      PMCID: PMC1288294          DOI: 10.1086/302638

Source DB:  PubMed          Journal:  Am J Hum Genet        ISSN: 0002-9297            Impact factor:   11.025


  24 in total

1.  Sequence-based exon prediction around the synaptophysin locus reveals a gene-rich area containing novel genes in human proximal Xp.

Authors:  S E Fisher; A Ciccodicola; K Tanaka; A Curci; S Desicato; M D'urso; I W Craig
Journal:  Genomics       Date:  1997-10-15       Impact factor: 5.736

2.  Oligophrenin-1 encodes a rhoGAP protein involved in X-linked mental retardation.

Authors:  P Billuart; T Bienvenu; N Ronce; V des Portes; M C Vinet; R Zemni; H Roest Crollius; A Carrié; F Fauchereau; M Cherry; S Briault; B Hamel; J P Fryns; C Beldjord; A Kahn; C Moraine; J Chelly
Journal:  Nature       Date:  1998-04-30       Impact factor: 49.962

Review 3.  Interplay between Ras-related and heterotrimeric GTP binding proteins: lifestyles of the BIG and little.

Authors:  G M Bokoch
Journal:  FASEB J       Date:  1996-09       Impact factor: 5.191

4.  Genetic localisation of mental retardation with spastic diplegia to the pericentromeric region of the X chromosome: X inactivation in female carriers.

Authors:  F Martínez; M Tomás; J M Millán; A Fernández; F Palau; F Prieto
Journal:  J Med Genet       Date:  1998-04       Impact factor: 6.318

5.  HPRT-APRT-deficient mice are not a model for lesch-nyhan syndrome.

Authors:  S J Engle; D E Womer; P M Davies; G Boivin; A Sahota; H A Simmonds; P J Stambrook; J A Tischfield
Journal:  Hum Mol Genet       Date:  1996-10       Impact factor: 6.150

6.  A common molecular basis for three inherited kidney stone diseases.

Authors:  S E Lloyd; S H Pearce; S E Fisher; K Steinmeyer; B Schwappach; S J Scheinman; B Harding; A Bolino; M Devoto; P Goodyer; S P Rigden; O Wrong; T J Jentsch; I W Craig; R V Thakker
Journal:  Nature       Date:  1996-02-01       Impact factor: 49.962

7.  A calcium channel mutation causing hypokalemic periodic paralysis.

Authors:  K Jurkat-Rott; F Lehmann-Horn; A Elbaz; R Heine; R G Gregg; K Hogan; P A Powers; P Lapie; J E Vale-Santos; J Weissenbach
Journal:  Hum Mol Genet       Date:  1994-08       Impact factor: 6.150

8.  An L-type calcium-channel gene mutated in incomplete X-linked congenital stationary night blindness.

Authors:  T M Strom; G Nyakatura; E Apfelstedt-Sylla; H Hellebrand; B Lorenz; B H Weber; K Wutz; N Gutwillinger; K Rüther; B Drescher; C Sauer; E Zrenner; T Meitinger; A Rosenthal; A Meindl
Journal:  Nat Genet       Date:  1998-07       Impact factor: 38.330

9.  Impairment of synaptic vesicle clustering and of synaptic transmission, and increased seizure propensity, in synapsin I-deficient mice.

Authors:  L Li; L S Chin; O Shupliakov; L Brodin; T S Sihra; O Hvalby; V Jensen; D Zheng; J O McNamara; P Greengard
Journal:  Proc Natl Acad Sci U S A       Date:  1995-09-26       Impact factor: 11.205

10.  Mutations in GDI1 are responsible for X-linked non-specific mental retardation.

Authors:  P D'Adamo; A Menegon; C Lo Nigro; M Grasso; M Gulisano; F Tamanini; T Bienvenu; A K Gedeon; B Oostra; S K Wu; A Tandon; F Valtorta; W E Balch; J Chelly; D Toniolo
Journal:  Nat Genet       Date:  1998-06       Impact factor: 38.330

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  10 in total

Review 1.  Movement disorders in mitochondrial disease.

Authors:  Roula Ghaoui; Carolyn M Sue
Journal:  J Neurol       Date:  2018-01-06       Impact factor: 4.849

Review 2.  HSD10 disease: clinical consequences of mutations in the HSD17B10 gene.

Authors:  Johannes Zschocke
Journal:  J Inherit Metab Dis       Date:  2011-11-30       Impact factor: 4.982

3.  The reduced expression of the HADH2 protein causes X-linked mental retardation, choreoathetosis, and abnormal behavior.

Authors:  Claus Lenski; R Frank Kooy; Edwin Reyniers; Daniela Loessner; Ronald J A Wanders; Birgitta Winnepenninckx; Heide Hellebrand; Stefanie Engert; Charles E Schwartz; Alfons Meindl; Juliane Ramser
Journal:  Am J Hum Genet       Date:  2006-12-28       Impact factor: 11.025

4.  A novel HSD17B10 mutation impairing the activities of the mitochondrial RNase P complex causes X-linked intractable epilepsy and neurodevelopmental regression.

Authors:  Marni J Falk; Xiaowu Gai; Megumi Shigematsu; Elisa Vilardo; Ryuichi Takase; Elizabeth McCormick; Thomas Christian; Emily Place; Eric A Pierce; Mark Consugar; Howard B Gamper; Walter Rossmanith; Ya-Ming Hou
Journal:  RNA Biol       Date:  2016-03-07       Impact factor: 4.652

5.  Hydroxysteroid 17-Beta Dehydrogenase Type 10 Disease in Siblings.

Authors:  Annely Richardson; Gerard T Berry; Cheryl Garganta; Mary-Alice Abbott
Journal:  JIMD Rep       Date:  2016-06-14

6.  DIA1R is an X-linked gene related to Deleted In Autism-1.

Authors:  Azhari Aziz; Sean P Harrop; Naomi E Bishop
Journal:  PLoS One       Date:  2011-01-17       Impact factor: 3.240

7.  A novel mutation in the HSD17B10 gene of a 10-year-old boy with refractory epilepsy, choreoathetosis and learning disability.

Authors:  Laurie H Seaver; Xue-Ying He; Keith Abe; Tina Cowan; Gregory M Enns; Lawrence Sweetman; Manfred Philipp; Sansan Lee; Mazhar Malik; Song-Yu Yang
Journal:  PLoS One       Date:  2011-11-22       Impact factor: 3.240

8.  Investigation of sex differences in the expression of RORA and its transcriptional targets in the brain as a potential contributor to the sex bias in autism.

Authors:  Valerie W Hu; Tewarit Sarachana; Rachel M Sherrard; Kristen M Kocher
Journal:  Mol Autism       Date:  2015-05-13       Impact factor: 7.509

9.  Genome-wide identification of transcriptional targets of RORA reveals direct regulation of multiple genes associated with autism spectrum disorder.

Authors:  Tewarit Sarachana; Valerie W Hu
Journal:  Mol Autism       Date:  2013-05-22       Impact factor: 7.509

10.  TM4SF10 gene sequencing in XLMR patients identifies common polymorphisms but no disease-associated mutation.

Authors:  Christiane Christophe-Hobertus; Frank Kooy; Jozef Gecz; Marc J Abramowicz; Elke Holinski-Feder; Charles Schwartz; Daniel Christophe
Journal:  BMC Med Genet       Date:  2004-09-02       Impact factor: 2.103

  10 in total

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