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Détail de l'auteur
Auteur L. KAUFMAN |
Documents disponibles écrits par cet auteur (1)
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The genetic basis of non-syndromic intellectual disability: a review / L. KAUFMAN in Journal of Neurodevelopmental Disorders, 2-4 (December 2010)
[article]
Titre : The genetic basis of non-syndromic intellectual disability: a review Type de document : Texte imprimé et/ou numérique Auteurs : L. KAUFMAN, Auteur ; M. AYUB, Auteur ; J. B. VINCENT, Auteur Article en page(s) : p.182-209 Langues : Anglais (eng) Index. décimale : PER Périodiques Résumé : Intellectual disability (ID), also referred to as mental retardation (MR), is frequently the result of genetic mutation. Where ID is present together with additional clinical symptoms or physical anomalies, there is often sufficient information available for the diagnosing physician to identify a known syndrome, which may then educe the identification of the causative defect. However, where co-morbid features are absent, narrowing down a specific gene can only be done by 'brute force' using the latest molecular genetic techniques. Here we attempt to provide a systematic review of genetic causes of cases of ID where no other symptoms or co-morbid features are present, or non-syndromic ID. We attempt to summarize commonalities between the genes and the molecular pathways of their encoded proteins. Since ID is a common feature of autism, and conversely autistic features are frequently present in individuals with ID, we also look at possible overlaps in genetic etiology with non-syndromic ID. En ligne : http://dx.doi.org/10.1007/s11689-010-9055-2 Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=342
in Journal of Neurodevelopmental Disorders > 2-4 (December 2010) . - p.182-209[article] The genetic basis of non-syndromic intellectual disability: a review [Texte imprimé et/ou numérique] / L. KAUFMAN, Auteur ; M. AYUB, Auteur ; J. B. VINCENT, Auteur . - p.182-209.
Langues : Anglais (eng)
in Journal of Neurodevelopmental Disorders > 2-4 (December 2010) . - p.182-209
Index. décimale : PER Périodiques Résumé : Intellectual disability (ID), also referred to as mental retardation (MR), is frequently the result of genetic mutation. Where ID is present together with additional clinical symptoms or physical anomalies, there is often sufficient information available for the diagnosing physician to identify a known syndrome, which may then educe the identification of the causative defect. However, where co-morbid features are absent, narrowing down a specific gene can only be done by 'brute force' using the latest molecular genetic techniques. Here we attempt to provide a systematic review of genetic causes of cases of ID where no other symptoms or co-morbid features are present, or non-syndromic ID. We attempt to summarize commonalities between the genes and the molecular pathways of their encoded proteins. Since ID is a common feature of autism, and conversely autistic features are frequently present in individuals with ID, we also look at possible overlaps in genetic etiology with non-syndromic ID. En ligne : http://dx.doi.org/10.1007/s11689-010-9055-2 Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=342