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.
Rampone, B., Filipeschi, M., DI MARTINO, M., Marrelli, D., Pedrazzani, C., Grimaldi, L., et al. (2008). Mayer-Rokitansky-Küster-Hauser syndrome presenting as vaginal atresia: report of two cases. IL GIORNALE DI CHIRURGIA, 29(4), 165-167.
Mayer-Rokitansky-Küster-Hauser syndrome presenting as vaginal atresia: report of two cases
RAMPONE, BERNARDINO;DI MARTINO, MARIANNA;MARRELLI, DANIELE;PEDRAZZANI, CORRADO;GRIMALDI, LUCA;CERULLO, GUIDO;CARUSO, STEFANO;PINTO, ENRICO;ROVIELLO, FRANCO
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.
| File | Dimensione | Formato | |
|---|---|---|---|
|
G CHIR 2008 MRKH syndrome.pdf
non disponibili
Tipologia:
Post-print
Licenza:
NON PUBBLICO - Accesso privato/ristretto
Dimensione
201.75 kB
Formato
Adobe PDF
|
201.75 kB | Adobe PDF | Visualizza/Apri Richiedi una copia |
I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.
https://hdl.handle.net/11365/20252
Attenzione
Attenzione! I dati visualizzati non sono stati sottoposti a validazione da parte dell'ateneo