Your browser doesn't support javascript.
loading
Mostrar: 20 | 50 | 100
Resultados 1 - 1 de 1
Filtrar
Adicionar filtros








Intervalo de ano
1.
Indian J Pediatr ; 2008 Jun; 75(6): 629-31
Artigo em Inglês | IMSEAR | ID: sea-82908

RESUMO

Triple X syndrome is a rare numerical chromosomal anomaly, occurring as a result of non dysjunction in meiosis I. Most cases have neurodevelopmental defects and functional problems. We report two cases diagnosed in our centre. The first was a fetus with cleft lip and palate, 47, XXX was identified by Fetal Blood Sampling. The second was a child with multisystem anomaly including cleft lip and palate, whose karyotype also revealed 47, XXX. Though isolated cases of associated abnormalities have been reported there have not been consistent phenotypic changes reported with this condition.


Assuntos
Anormalidades Múltiplas/genética , Adulto , Criança , Cromossomos Humanos X/genética , Fenda Labial/genética , Fissura Palatina/genética , Feminino , Humanos , Cariotipagem , Fenótipo , Gravidez , Aberrações dos Cromossomos Sexuais , Ultrassonografia Pré-Natal
SELEÇÃO DE REFERÊNCIAS
DETALHE DA PESQUISA