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PMID: 22713806 Published · ppublish English Case Reports Journal Article Research Support, Non-U.S. Gov't

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

European journal of human genetics : EJHG ·Vol. 21 ·No. 1 ·2013-01-00 ·Pages 82-8

Thevenon J, Callier P, Andrieux J, Delobel B, David A, Sukno S, Minot D, Mosca Anne L, Marle N, Sanlaville D, Bonnet M, Masurel-Paulet A, Levy F, Gaunt L, Farrell S, Le Caignec C, Toutain A, Carmignac V, Mugneret F, Clayton-Smith J, Thauvin-Robinet C, Faivre L

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.

MeSH Terms
Adaptor Proteins, Signal Transducing/genetics Apraxias/etiology,genetics Child Child, Preschool Chromosome Deletion Chromosomes, Human, Pair 12 Family Female France Genetic Predisposition to Disease Humans In Situ Hybridization, Fluorescence Language Development Disorders/genetics Male Nerve Tissue Proteins/genetics Pregnancy Speech
Chemicals
Adaptor Proteins, Signal Transducing ERC1 protein, human Nerve Tissue Proteins
Authors & Affiliations
22 authors, click to expand affiliations / ORCID
Thevenon Julien
Centre de Génétique et Centre de Référence «Anomalies du Développement et Syndromes Malformatifs», Hôpital d'Enfants, CHU Dijon, Dijon, France.
Callier Patrick
Andrieux Joris
Delobel Bruno
David Albert
Sukno Sylvie
Minot Delphine
Mosca Anne Laure
Marle Nathalie
Sanlaville Damien
Bonnet Marlène
Masurel-Paulet Alice
Levy Fabienne
Gaunt Lorraine
Farrell Sandra
Le Caignec Cédric
Toutain Annick
Carmignac Virginie
Mugneret Francine
Clayton-Smith Jill
Thauvin-Robinet Christel
Faivre Laurence
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Article Info
Journal
European journal of human genetics : EJHG
Abbr.
Eur J Hum Genet
ISSN
1476-5438
Published
2013-01-00
Epub
2012-00-20
Pages
82-8
Language
English
Region
England
NLM ID
9302235
PMCID
PMC3522191
Subset
IM
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