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Pediatr Clin North Am ; 71(2): 179-197, 2024 Apr.
Artículo en Inglés | MEDLINE | ID: mdl-38423715

RESUMEN

Autism spectrum disorder (ASD) is clinically and etiologically heterogeneous. A causal genetic variant can be identified in approximately 20% to 25% of affected individuals with current clinical genetic testing, and all patients with an ASD diagnosis should be offered genetic etiologic evaluation. We suggest that exome sequencing with copy number variant coverage should be the first-line etiologic evaluation for ASD. Neuroimaging, neurophysiologic, metabolic, and other biochemical evaluations can provide insight into the pathophysiology of ASD but should be recommended in the appropriate clinical circumstances.


Asunto(s)
Trastorno del Espectro Autista , Niño , Humanos , Trastorno del Espectro Autista/etiología , Trastorno del Espectro Autista/genética , Variaciones en el Número de Copia de ADN , Pruebas Genéticas , Neuroimagen
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