[article]
| Titre : |
Additive Effect of Variably Penetrant 22q11.2 Duplication and Pathogenic Mutations in Autism Spectrum Disorder: To Which Extent Does the Tree Hide the Forest? |
| Type de document : |
Texte imprimé et/ou numérique |
| Auteurs : |
Caroline DEMILY, Auteur ; G. LESCA, Auteur ; A. POISSON, Auteur ; M. TILL, Auteur ; Giulia BARCIA, Auteur ; N. CHATRON, Auteur ; Damien SANLAVILLE, Auteur ; A. MUNNICH, Auteur |
| Article en page(s) : |
p.2886-2889 |
| Langues : |
Anglais (eng) |
| Mots-clés : |
22q11.2 duplication Autism spectrum disorders Epilepsy Genetic counseling Incomplete penetrance Next generation sequencing |
| Index. décimale : |
PER Périodiques |
| Résumé : |
The 22q11.2 duplication is a variably penetrant copy number variant (CNV) associated with a broad spectrum of clinical manifestations including autism spectrum disorders (ASD), and epilepsy. Here, we report on pathogenic HUWE1 and KIF1A mutations in two severely affected ASD/ID participants carrying a 22q11.2 duplication. Based on previous studies, this CNV was originally considered as disease-causing. Yet, owing to their clinical severity, the participants were further investigated by next generation sequencing and eventually found to carry pathogenic mutations in HUWE1 and KIF1A respectively. We suggest giving consideration to additive effect of 22q11.2 duplication and pathogenic mutations when clinical presentation is either unusually severe or associated with atypical features. Caution should be exercised when delivering genetic counseling for variably penetrant CNVs, as uncertain penetrance of this CNV may lead to ignore additive pathogenic mutations. Systematic panel or exome sequencing of known ASD genes should be recommended when counseling families of patients carrying variably penetrant CNV. |
| En ligne : |
http://dx.doi.org/10.1007/s10803-018-3552-7 |
| Permalink : |
https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=367 |
in Journal of Autism and Developmental Disorders > 48-8 (August 2018) . - p.2886-2889
[article] Additive Effect of Variably Penetrant 22q11.2 Duplication and Pathogenic Mutations in Autism Spectrum Disorder: To Which Extent Does the Tree Hide the Forest? [Texte imprimé et/ou numérique] / Caroline DEMILY, Auteur ; G. LESCA, Auteur ; A. POISSON, Auteur ; M. TILL, Auteur ; Giulia BARCIA, Auteur ; N. CHATRON, Auteur ; Damien SANLAVILLE, Auteur ; A. MUNNICH, Auteur . - p.2886-2889. Langues : Anglais ( eng) in Journal of Autism and Developmental Disorders > 48-8 (August 2018) . - p.2886-2889
| Mots-clés : |
22q11.2 duplication Autism spectrum disorders Epilepsy Genetic counseling Incomplete penetrance Next generation sequencing |
| Index. décimale : |
PER Périodiques |
| Résumé : |
The 22q11.2 duplication is a variably penetrant copy number variant (CNV) associated with a broad spectrum of clinical manifestations including autism spectrum disorders (ASD), and epilepsy. Here, we report on pathogenic HUWE1 and KIF1A mutations in two severely affected ASD/ID participants carrying a 22q11.2 duplication. Based on previous studies, this CNV was originally considered as disease-causing. Yet, owing to their clinical severity, the participants were further investigated by next generation sequencing and eventually found to carry pathogenic mutations in HUWE1 and KIF1A respectively. We suggest giving consideration to additive effect of 22q11.2 duplication and pathogenic mutations when clinical presentation is either unusually severe or associated with atypical features. Caution should be exercised when delivering genetic counseling for variably penetrant CNVs, as uncertain penetrance of this CNV may lead to ignore additive pathogenic mutations. Systematic panel or exome sequencing of known ASD genes should be recommended when counseling families of patients carrying variably penetrant CNV. |
| En ligne : |
http://dx.doi.org/10.1007/s10803-018-3552-7 |
| Permalink : |
https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=367 |
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