Chromosomal abnormalities and autism
Egyptian Journal of Medical Human Genetics [The]. 2016; 17 (1): 57-62
en Inglés
| IMEMR
| ID: emr-176214
ABSTRACT
Background:
Autism is a neurodevelopmental disorder characterized by clinical, etiologic and genetic heterogeneity. Many surveys revealed cytogenetically visible chromosomal abnormalities in 7.4% of autistic patients documented as well as several submicroscopic variants. This study had been conducted to identify some aspects that might be involved in the pathogenesis of autism which is necessary for offering proper genetic counseling to families of autistic patients and their role in the prenatal diagnosis of autism
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Índice:
IMEMR (Mediterraneo Oriental)
Asunto principal:
Estudios Transversales
/
Aberraciones Cromosómicas
/
Cariotipo
/
Cariotipificación
Tipo de estudio:
Estudio de prevalencia
Límite:
Niño
/
Child, preschool
/
Femenino
/
Humanos
/
Masculino
Idioma:
Inglés
Revista:
Egypt. J. Med. Hum. Genet.
Año:
2016
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