Currarino triad with Mullerian duct anomaly in mother and daughter without MNX1 gene mutation
Annals of Surgical Treatment and Research
;
: 49-52, 2016.
Article
Dans Anglais
| WPRIM
| ID: wpr-59523
ABSTRACT
The Currarino triad is a unique complex of congenital caudal anomalies, including anorectal malformation, sacral bony defect and presacral mass. This triad may be associated with Mullerian duct anomalies, such as duplication of the vagina and uterus. Each of these diseases has a familial tendency and sometimes coexist within families. But, when coexisting in familial cases, nearly all reported cases revealed mutations of the motor neuron and pancreas homeobox 1 (MNX1) gene. Familial cases of Currarino triad combined with Mullerian duct anomaly without MNX1 gene mutation are very rare. Here we report cases of mother and daughter, who had Currarino triad and Mullerian duct anomaly without MNX1 gene mutation, along with a brief literature review.
Texte intégral:
Disponible
Indice:
WPRIM (Pacifique occidental)
Sujet Principal:
Pancréas
/
Utérus
/
Vagin
/
Famille nucléaire
/
Gènes homéotiques
/
Mères
/
Motoneurones
/
Canaux de Müller
Limites du sujet:
Humains
langue:
Anglais
Texte intégral:
Annals of Surgical Treatment and Research
Année:
2016
Type:
Article
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