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Review

Role of Genetics in the Etiology of Autistic Spectrum Disorder: Towards a Hierarchical Diagnostic Strategy

1
Pôle Hospitalo-Universitaire de Psychiatrie de l’Enfant et de l’Adolescent (PHUPEA), University of Rennes 1 and Centre Hospitalier Guillaume Régnier, 35200 Rennes, France
2
Service de Génétique Clinique, Centre de Référence Maladies Rares Anomalies du Développement (Centre Labellisé pour les Anomalies du Développement de l’Ouest: CLAD Ouest), Hôpital Sud, Centre Hospitalier Universitaire de Rennes, 35200 Rennes, France
3
Hospital-University Department of Child and Adolescent Psychiatry, Pitié-Salpétrière Hospital, Paris 6 University, 75013 Paris, France
4
Division of Child and Adolescent Neuropsychiatry, University Hospital of Siena, 53100 Siena, Italy
5
Laboratory of Psychology of Perception, University Paris Descartes, 75270 Paris, France
*
Author to whom correspondence should be addressed.
Academic Editor: Merlin G. Butler
Int. J. Mol. Sci. 2017, 18(3), 618; https://0-doi-org.brum.beds.ac.uk/10.3390/ijms18030618
Received: 13 December 2016 / Revised: 17 February 2017 / Accepted: 20 February 2017 / Published: 12 March 2017
Progress in epidemiological, molecular and clinical genetics with the development of new techniques has improved knowledge on genetic syndromes associated with autism spectrum disorder (ASD). The objective of this article is to show the diversity of genetic disorders associated with ASD (based on an extensive review of single-gene disorders, copy number variants, and other chromosomal disorders), and consequently to propose a hierarchical diagnostic strategy with a stepwise evaluation, helping general practitioners/pediatricians and child psychiatrists to collaborate with geneticists and neuropediatricians, in order to search for genetic disorders associated with ASD. The first step is a clinical investigation involving: (i) a child psychiatric and psychological evaluation confirming autism diagnosis from different observational sources and assessing autism severity; (ii) a neuropediatric evaluation examining neurological symptoms and developmental milestones; and (iii) a genetic evaluation searching for dysmorphic features and malformations. The second step involves laboratory and if necessary neuroimaging and EEG studies oriented by clinical results based on clinical genetic and neuropediatric examinations. The identification of genetic disorders associated with ASD has practical implications for diagnostic strategies, early detection or prevention of co-morbidity, specific treatment and follow up, and genetic counseling. View Full-Text
Keywords: autism; genetic disorders; hierarchical diagnostic strategy; child psychiatric and psychological assessment; clinical genetics; neuropediatric evaluation autism; genetic disorders; hierarchical diagnostic strategy; child psychiatric and psychological assessment; clinical genetics; neuropediatric evaluation
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MDPI and ACS Style

Robert, C.; Pasquier, L.; Cohen, D.; Fradin, M.; Canitano, R.; Damaj, L.; Odent, S.; Tordjman, S. Role of Genetics in the Etiology of Autistic Spectrum Disorder: Towards a Hierarchical Diagnostic Strategy. Int. J. Mol. Sci. 2017, 18, 618. https://0-doi-org.brum.beds.ac.uk/10.3390/ijms18030618

AMA Style

Robert C, Pasquier L, Cohen D, Fradin M, Canitano R, Damaj L, Odent S, Tordjman S. Role of Genetics in the Etiology of Autistic Spectrum Disorder: Towards a Hierarchical Diagnostic Strategy. International Journal of Molecular Sciences. 2017; 18(3):618. https://0-doi-org.brum.beds.ac.uk/10.3390/ijms18030618

Chicago/Turabian Style

Robert, Cyrille, Laurent Pasquier, David Cohen, Mélanie Fradin, Roberto Canitano, Léna Damaj, Sylvie Odent, and Sylvie Tordjman. 2017. "Role of Genetics in the Etiology of Autistic Spectrum Disorder: Towards a Hierarchical Diagnostic Strategy" International Journal of Molecular Sciences 18, no. 3: 618. https://0-doi-org.brum.beds.ac.uk/10.3390/ijms18030618

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