Results 91 to 100 of about 262,079 (155)

Síndrome de Mayer-von Rokitansky-Küster-Hauser

Revista Universitas Medica, 2013
Introducción: el síndrome de Mayer-von Rokitansky-Küster-Hauser (MRKH) ocurre aproximadamente en una de cada cinco mil mujeres nacidas vivas y es la causa más común de ausencia congénita de vagina. Método: se presentan dos casos manejados quirúrgicamente
Gabriel Andrés Barbosa Ramírez, Luis Jorge Lombana, Leila Quintero   +2 more
doaj  

Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome. Diagnostic and therapeutic approach of a rare disease

, 2019
Introduccion: El síndrome de Mayer-Rokitansky-Küster-Hauser se caracteriza por la agenesia de vagina y útero en una mujer con desarrollo normal de caracteres sexuales y amenorrea primaria.
Martín, Silvia, Noguero, Rosario, Muñoz, María del Mar   +2 more
core  

Posterior mediastinal Müllerian cyst in a patient with Mayer-Rokitansky-Küster-Hauser syndrome: a case report. [PDF]

J Surg Case Rep
Aleksandrov O, Patrini D, De Luca M, Moore D, Gkikas A, Jayathilaka A.   +5 more
europepmc   +1 more source

Vaginal Agenesis (Mayer-Rokitansky-Kuster-Hauser Syndrome) Presenting with Exertional Dyspnoea, Fatigue and Intermittent Palpitations. [PDF]

Eur J Case Rep Intern Med
Dave P, Sharma S, Nagarkar M, Saklecha A, Jagtap A.   +4 more
europepmc   +1 more source

Menarche in the third decade: congenital adrenal hyperplasia masquerading as Mayer-Rokitansky-Küster-Hauser syndrome. [PDF]

JCEM Case Rep
A V Alekya L, Mashetty S, Guddeti A, Manasa CVS, Bora A, Hari'Kumar KVS.   +5 more
europepmc   +1 more source

Rare Association of Mayer-Rokitansky-Kuster-Hauser Syndrome with Rectovestibular Fistula and Colonic Atresia. [PDF]

J Indian Assoc Pediatr Surg
Pais A, Karkera P, Bendre PS, Sanglikar S, Pikale H, Bodhanwala M.   +5 more
europepmc   +1 more source

Síndrome de Mayer-Rokitansky-Küster-Hauser: da abordagem ao tratamento [PDF]

A Síndrome de Mayer-Rokitansky-Küster-Hauser (MRKH) é uma condição rara que atinge mulheres, afetando sua saúde física e emocional. Ela pode ser dividida em dois tipos: tipo I (aplasia congênita do útero e da parte superior da vagina); e tipo II (aplasia
de Andrade Reis, Letícia, de Faria Huguenin, Tássio, Marques, Juliana, Botelho Pacheco Pires, Thaís   +3 more
core  

Robotic-assisted laparoscopic excision of rudimentary uteri for chronic pelvic pain in Mayer-Rokitansky-Küster-Hauser syndrome: a case report. [PDF]

Int J Surg Case Rep
Csorba R, Buderath P, Rawitzer J, Almasarweh SE, Britten MW, Atas Elfrink Z.   +5 more
europepmc   +1 more source

Mayer-Rokitansky-Küster-Hauser syndrome type II. Case report. [PDF]

JBRA Assist Reprod
Calle JJR.
europepmc   +1 more source

Spectrum of Genitourinary Dysgenesis on Magnetic Resonance Imaging: A Case Series of Zinner and Mayer-Rokitansky-Küster-Hauser Syndromes. [PDF]

Cureus
Trivedi VS, Tembhekar NG, Rathi V, Bhutada NR, Disawal AG, Parate R.   +5 more
europepmc   +1 more source