Mayer-Rokitansky-Küster-Hauser syndrome (MRKH syndrome) is characterized by Müllerian duct structures agenesis: the vagina atresia is the commonest variant. There can be some anomalies associated, such as renal, skeletal, spine malformations and others. Patients with MRKH can show different presentation from newborn period to adolescence. We report our experience in treatment of the vaginal atresia presenting in two young girls as a sign of MRKH syndrome

Mayer-Rokitansky-Küster-Hauser syndrome presenting as vaginal atresia: report of two cases / Rampone, B., Filippeschi, M., Di Martino, M., Marrelli, D., Pedrazzani, C., Grimaldi, L., Cerullo, G., Caruso, S., Pinto, E., Roviello, F.. - In: IL GIORNALE DI CHIRURGIA. - ISSN 0391-9005. - STAMPA. - 29:4(2008), pp. 165-167.

Mayer-Rokitansky-Küster-Hauser syndrome presenting as vaginal atresia: report of two cases

PEDRAZZANI C;
2008-01-01

Abstract

Mayer-Rokitansky-Küster-Hauser syndrome (MRKH syndrome) is characterized by Müllerian duct structures agenesis: the vagina atresia is the commonest variant. There can be some anomalies associated, such as renal, skeletal, spine malformations and others. Patients with MRKH can show different presentation from newborn period to adolescence. We report our experience in treatment of the vaginal atresia presenting in two young girls as a sign of MRKH syndrome
2008
4
Rampone, B; Filippeschi, M; Di Martino, M; Marrelli, D; Pedrazzani, C; Grimaldi, L; Cerullo, G; Caruso, S; Pinto, E; Roviello, F
Mayer-Rokitansky-Küster-Hauser syndrome presenting as vaginal atresia: report of two cases / Rampone, B., Filippeschi, M., Di Martino, M., Marrelli, D., Pedrazzani, C., Grimaldi, L., Cerullo, G., Caruso, S., Pinto, E., Roviello, F.. - In: IL GIORNALE DI CHIRURGIA. - ISSN 0391-9005. - STAMPA. - 29:4(2008), pp. 165-167.
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11572/480247
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