The Experts below are selected from a list of 15 Experts worldwide ranked by ideXlab platform
F. Roviello - One of the best experts on this subject based on the ideXlab platform.
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Mayer-Rokitansky-Küster-Hauser syndrome presenting as Vaginal Atresia: report of two cases.
Il Giornale di chirurgia, 2008Co-Authors: Bernardino Rampone, M. Filippeschi, M. Di Martino, Daniele Marrelli, Corrado Pedrazzani, L. Grimaldi, Guido Cerullo, Stefano Caruso, Enrico Pinto, F. RovielloAbstract:Mayer-Rokitansky-Kiister-Hauser syndrome (MRKH syndrome) is characterized by Miillerian 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.
Roviello F - One of the best experts on this subject based on the ideXlab platform.
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Mayer-Rokitansky-Küster-Hauser syndrome presenting as Vaginal Atresia: report of two cases
2008Co-Authors: Rampone B, Filippeschi M, Di Martino M, Marrelli D, Pedrazzani C, Grimaldi L, Cerullo G, Caruso S, Pinto E, Roviello FAbstract:Mayer-Rokitansky-K\ufcster-Hauser syndrome (MRKH syndrome) is characterized by M\ufcllerian 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
Bernardino Rampone - One of the best experts on this subject based on the ideXlab platform.
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Mayer-Rokitansky-Küster-Hauser syndrome presenting as Vaginal Atresia: report of two cases.
Il Giornale di chirurgia, 2008Co-Authors: Bernardino Rampone, M. Filippeschi, M. Di Martino, Daniele Marrelli, Corrado Pedrazzani, L. Grimaldi, Guido Cerullo, Stefano Caruso, Enrico Pinto, F. RovielloAbstract:Mayer-Rokitansky-Kiister-Hauser syndrome (MRKH syndrome) is characterized by Miillerian 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 - One of the best experts on this subject based on the ideXlab platform.
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Mayer-Rokitansky-Küster-Hauser syndrome presenting as Vaginal Atresia: report of two cases
2008Co-Authors: Rampone B, Filippeschi M, Di Martino M, Marrelli D, Pedrazzani C, Grimaldi L, Cerullo G, Caruso S, Pinto E, Roviello FAbstract:Mayer-Rokitansky-K\ufcster-Hauser syndrome (MRKH syndrome) is characterized by M\ufcllerian 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
Marrelli D - One of the best experts on this subject based on the ideXlab platform.
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Mayer-Rokitansky-Küster-Hauser syndrome presenting as Vaginal Atresia: report of two cases
2008Co-Authors: Rampone B, Filippeschi M, Di Martino M, Marrelli D, Pedrazzani C, Grimaldi L, Cerullo G, Caruso S, Pinto E, Roviello FAbstract:Mayer-Rokitansky-K\ufcster-Hauser syndrome (MRKH syndrome) is characterized by M\ufcllerian 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
