Chromosomal abnormalities and autism
Egyptian Journal of Medical Human Genetics [The]. 2016; 17 (1): 57-62
em Inglês
| 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
Buscar no Google
Índice:
IMEMR (Mediterrâneo Oriental)
Assunto principal:
Estudos Transversais
/
Aberrações Cromossômicas
/
Cariótipo
/
Cariotipagem
Tipo de estudo:
Estudo de prevalência
Limite:
Criança
/
Criança, pré-escolar
/
Feminino
/
Humanos
/
Masculino
Idioma:
Inglês
Revista:
Egypt. J. Med. Hum. Genet.
Ano de publicação:
2016
Similares
MEDLINE
...
LILACS
LIS