Semilobar holoprosencephaly in Seckel syndrome.
Indian J Pediatr
;
2008 May; 75(5): 519-20
Artículo
en Inglés
| IMSEAR
| ID: sea-83251
ABSTRACT
Seckel syndrome is a rare genetic disorder with autosomal recessive inheritance. It is associated with many CNS anomalies along with involvement of other systems. We present a case of Seckel syndrome with semilobar holoprosencephaly as associated CNS anomaly, which to the best of our knowledge has not been reported earlier.
Texto completo:
Disponible
Índice:
IMSEAR (Asia Sudoriental)
Asunto principal:
Síndrome
/
Anomalías Múltiples
/
Humanos
/
Masculino
/
Recién Nacido
/
Holoprosencefalia
/
Enanismo
/
Discapacidad Intelectual
/
Microcefalia
Idioma:
Inglés
Revista:
Indian J Pediatr
Año:
2008
Tipo del documento:
Artículo
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