Neurobehavioral Profile and Brain Imaging Study of the 22q13.3 Deletion Syndrome in Childhood

The 22q13.3 deletion syndrome (Online Mendelian Inheritance in Man No. 606232) is a neurodevelopmental disorder that includes hypotonia, severely impaired development of speech and language, autistic-like behavior, and minor dysmorphic features. Although the number of reported cases is increasing, t...

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Veröffentlicht in:	Pediatrics (Evanston) 2008-08, Vol.122 (2), p.e376-e382
Hauptverfasser:	Philippe, Anne, Boddaert, Nathalie, Vaivre-Douret, Laurence, Robel, Laurence, Danon-Boileau, Laurent, Malan, Valerie, de Blois, Marie-Christine, Heron, Delphine, Colleaux, Laurence, Golse, Bernard, Zilbovicius, Monica, Munnich, Arnold
Format:	Artikel
Sprache:	eng
Schlagworte:	Brain Brain Diseases - diagnosis Brain Diseases - genetics Child Child, Preschool Children & youth Chromosome Deletion Chromosomes, Human, Pair 22 Cognition Disorders - diagnosis Cognition Disorders - genetics Cohort Studies Developmental Disabilities - diagnosis Developmental Disabilities - genetics Diagnostic Imaging - methods Female Heterozygote Humans Intellectual Disability - diagnosis Intellectual Disability - genetics Magnetic Resonance Imaging Male Medical disorders Neuropsychological Tests Neuropsychology NMR Nuclear magnetic resonance Pediatrics Positron-Emission Tomography Prognosis Psychology Psychomotor Disorders - diagnosis Psychomotor Disorders - genetics Speech Disorders - diagnosis Speech Disorders - genetics
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