Literature DB >> 22713806

12p13.33 microdeletion including ELKS/ERC1, a new locus associated with childhood apraxia of speech.

Julien Thevenon1, Patrick Callier, Joris Andrieux, Bruno Delobel, Albert David, Sylvie Sukno, Delphine Minot, Laure Mosca Anne, Nathalie Marle, Damien Sanlaville, Marlène Bonnet, Alice Masurel-Paulet, Fabienne Levy, Lorraine Gaunt, Sandra Farrell, Cédric Le Caignec, Annick Toutain, Virginie Carmignac, Francine Mugneret, Jill Clayton-Smith, Christel Thauvin-Robinet, Laurence Faivre.   

Abstract

Speech sound disorders are heterogeneous conditions, and sporadic and familial cases have been described. However, monogenic inheritance explains only a small proportion of such disorders, in particular in cases with childhood apraxia of speech (CAS). Deletions of <5 Mb involving the 12p13.33 locus is one of the least commonly deleted subtelomeric regions. Only four patients have been reported with such a deletion diagnosed with fluorescence in situ hybridisation telomere analysis or array CGH. To further delineate this rare microdeletional syndrome, a French collaboration together with a search in the Decipher database allowed us to gather nine new patients with a 12p13.33 subtelomeric or interstitial rearrangement identified by array CGH. Speech delay was found in all patients, which could be defined as CAS when patients had been evaluated by a speech therapist (5/9 patients). Intellectual deficiency was found in 5/9 patients only, and often associated with psychiatric manifestations of various severity. Two such deletions were inherited from an apparently healthy parent, but reevaluation revealed abnormal speech production at least in childhood, suggesting variable expressivity. The ELKS/ERC1 gene, which encodes for a synaptic factor, is found in the smallest region of overlap. These results reinforce the hypothesis that deletions of the 12p13.33 locus may be responsible for variable phenotypes including CAS associated with neurobehavioural troubles and that the presence of CAS justifies a genetic work-up.

Entities:  

Mesh:

Substances:

Year:  2012        PMID: 22713806      PMCID: PMC3522191          DOI: 10.1038/ejhg.2012.116

Source DB:  PubMed          Journal:  Eur J Hum Genet        ISSN: 1018-4813            Impact factor:   4.246


  39 in total

1.  SRPX2 mutations in disorders of language cortex and cognition.

Authors:  Patrice Roll; Gabrielle Rudolf; Sandrine Pereira; Barbara Royer; Ingrid E Scheffer; Annick Massacrier; Maria-Paola Valenti; Nathalie Roeckel-Trevisiol; Sarah Jamali; Christophe Beclin; Caroline Seegmuller; Marie-Noëlle Metz-Lutz; Arnaud Lemainque; Marc Delepine; Christophe Caloustian; Anne de Saint Martin; Nadine Bruneau; Danièle Depétris; Marie-Geneviève Mattéi; Elisabeth Flori; Andrée Robaglia-Schlupp; Nicolas Lévy; Bernd A Neubauer; Rivka Ravid; Christian Marescaux; Samuel F Berkovic; Edouard Hirsch; Mark Lathrop; Pierre Cau; Pierre Szepetowski
Journal:  Hum Mol Genet       Date:  2006-02-23       Impact factor: 6.150

2.  Diagnostic criteria of developmental apraxia of speech used by clinical speech-language pathologists.

Authors:  Karen Forrest
Journal:  Am J Speech Lang Pathol       Date:  2003-08       Impact factor: 2.408

3.  Partial monosomy 12p13.1----13.3.

Authors:  D R Romain; J Goldsmith; L M Columbano-Green; C J Chapman; R H Smythe; R G Parfitt
Journal:  J Med Genet       Date:  1987-07       Impact factor: 6.318

4.  A familial cryptic subtelomeric deletion 12p with variable phenotypic effect.

Authors:  E Baker; L Hinton; D F Callen; E A Haan; A Dobbie; G R Sutherland
Journal:  Clin Genet       Date:  2002-03       Impact factor: 4.438

5.  Phenotypic variation in the del(12p) syndrome.

Authors:  J D Kivlin; R M Fineman; M S Williams
Journal:  Am J Med Genet       Date:  1985-12

6.  Prevalence of specific language impairment in kindergarten children.

Authors:  J B Tomblin; N L Records; P Buckwalter; X Zhang; E Smith; M O'Brien
Journal:  J Speech Lang Hear Res       Date:  1997-12       Impact factor: 2.297

7.  The prevalence of autistic spectrum disorders in adolescents with a history of specific language impairment (SLI).

Authors:  Gina Conti-Ramsden; Zoë Simkin; Nicola Botting
Journal:  J Child Psychol Psychiatry       Date:  2006-06       Impact factor: 8.982

8.  A forkhead-domain gene is mutated in a severe speech and language disorder.

Authors:  C S Lai; S E Fisher; J A Hurst; F Vargha-Khadem; A P Monaco
Journal:  Nature       Date:  2001-10-04       Impact factor: 49.962

9.  Short arm deletion of chromosome 12: report of two new cases.

Authors:  E Orye; M Craen
Journal:  Humangenetik       Date:  1975-08-25

10.  Distal 12p deletion in a stillborn infant.

Authors:  A Baroncini; C Avellini; C Neri; A Forabosco
Journal:  Am J Med Genet       Date:  1990-07
View more
  26 in total

1.  A highly penetrant form of childhood apraxia of speech due to deletion of 16p11.2.

Authors:  Evelina Fedorenko; Angela Morgan; Elizabeth Murray; Annie Cardinaux; Cristina Mei; Helen Tager-Flusberg; Simon E Fisher; Nancy Kanwisher
Journal:  Eur J Hum Genet       Date:  2015-07-15       Impact factor: 4.246

Review 2.  Decoding the biology of language and its implications in language acquisition.

Authors:  D R Rahul; R Joseph Ponniah
Journal:  J Biosci       Date:  2019-03       Impact factor: 1.826

3.  Heterozygous deletion of the LRFN2 gene is associated with working memory deficits.

Authors:  Julien Thevenon; Céline Souchay; Gail K Seabold; Inna Dygai-Cochet; Patrick Callier; Sébastien Gay; Lucie Corbin; Laurence Duplomb; Christel Thauvin-Robinet; Alice Masurel-Paulet; Salima El Chehadeh; Magali Avila; Delphine Minot; Eric Guedj; Sophie Chancenotte; Marlène Bonnet; Daphne Lehalle; Ya-Xian Wang; Paul Kuentz; Frédéric Huet; Anne-Laure Mosca-Boidron; Nathalie Marle; Ronald S Petralia; Laurence Faivre
Journal:  Eur J Hum Genet       Date:  2015-10-21       Impact factor: 4.246

Review 4.  Genetic insights into the functional elements of language.

Authors:  Adam Szalontai; Katalin Csiszar
Journal:  Hum Genet       Date:  2013-06-08       Impact factor: 4.132

Review 5.  Insights into the genetic foundations of human communication.

Authors:  Sarah A Graham; Pelagia Deriziotis; Simon E Fisher
Journal:  Neuropsychol Rev       Date:  2015-01-18       Impact factor: 7.444

6.  Rebuilding essential active zone functions within a synapse.

Authors:  Chao Tan; Shan Shan H Wang; Giovanni de Nola; Pascal S Kaeser
Journal:  Neuron       Date:  2022-02-16       Impact factor: 18.688

Review 7.  DECIPHER: web-based, community resource for clinical interpretation of rare variants in developmental disorders.

Authors:  Ganesh J Swaminathan; Eugene Bragin; Eleni A Chatzimichali; Manuel Corpas; A Paul Bevan; Caroline F Wright; Nigel P Carter; Matthew E Hurles; Helen V Firth
Journal:  Hum Mol Genet       Date:  2012-09-08       Impact factor: 6.150

8.  Quantitative profiling of brain lipid raft proteome in a mouse model of fragile X syndrome.

Authors:  Magdalena Kalinowska; Catherine Castillo; Anna Francesconi
Journal:  PLoS One       Date:  2015-04-07       Impact factor: 3.240

9.  [Application of single nucleotide polymorphism microarray in clinical diagnosis of intellectual disability or retardation].

Authors:  Junjie Hu; Yeqing Qian; Yixi Sun; Jialing Yu; Yuqin Luo; Minyue Dong
Journal:  Zhejiang Da Xue Xue Bao Yi Xue Ban       Date:  2019-06-25

Review 10.  Neurogenomics of speech and language disorders: the road ahead.

Authors:  Pelagia Deriziotis; Simon E Fisher
Journal:  Genome Biol       Date:  2013-04-18       Impact factor: 13.583

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.