Background The vertebral defect, anal atresia, cardiac defect, tracheoesophageal
fistula/esophageal atresia, renal defect, and limb defect association and Mayer-Rokitansky …

OBJECTIVES: The Mayer–Rokitansky–Küester–Hauser (MRKH) syndrome can be either
isolated uterovaginal agenesis or associated with other organ anomalies. However, MRKH …

Atypical Mayer-Rokitansky-Kuster-Hauser syndrome with scoliosis, renal &anorectal
malformation - case report - Document - Gale OneFile: Health and Medicine Use this link to …

Abstract Coexistence of Mayer‐Rokitansky‐Küster‐Hauser syndrome and gonadal
dysgenesis is extremely rare, and a case of Mayer‐Rokitansky‐Küster‐Hauser syndrome …

OBJECTIVE: To report a case of Mayer-Rokitansky-Küster-Hauser syndrome (MRKH) with a
utero-ovarian inguinal hernia, and to present a review of the pertinent literature. DESIGN …

Abstract Background Mayer–Rokitansky–Kuster–Hauser (MRKH) syndrome is a congenital
condition characterized by aplasia of the vagina with or without concurrent uterine and/or …

Mayer–Rokitansky–Küster–Hauser (MRKH) syndrome is a congenital disorder of still
unknown etiology, characterized by uterovaginal agenesis and can be associated with …

Abstract Mayer Rokitansky Kuster Houser syndrome (MRKH syndrome) is characterized by
Mullerian duct structures agenesis, vaginal atresia being the commonest variant. It can be …

Congenital absence of uterus and vagina, Mayer–Rokitansky–Kuster–Hauser (MRKH)
syndrome, is mullerian agenesis and is the second most frequent cause of primary …

Abstract The Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome affects at least 1 out of
4500 women and has for a long time been considered as a sporadic anomaly. Congenital …