Clinical features of Mayer–Rokitansky–Küster–Haüser syndrome diagnosed at under 16 years old: results from a questionnaire survey conducted on all institutions of pediatric surgery and pediatric urology in Japan

[1] Londra L(2015)Mayer–Rokitansky–Kuster–Hauser–syndrome: a review Int J Womens Health 2 865-870

[2] Chuong FS(2007)Mayer–Rokitansky–Küster–Hauser (MRKH) syndrome Orphanet J Rare Dis 14 13-458

[3] Kolp L(2016)Vertebral defect, anal atresia, cardiac defect, tracheoesophageal fistula/esophageal atresia, renal defect, and limb defect association with Mayer–Rokitansky–Küster–Hauser syndrome in co-occurrence: two case reports and a review of the literature J Med Case Rep 21 374-302

[4] Morcel K(2013)Investigation of the freely available easy-to-use software ‘EZR’ for medical statistics Bone Marrow Transplant 48 452-565

[5] Camborieux L(2003)Contemporary issues in primary amenorrhea Obstet Gynecol Clin 30 287-2390

[6] Guerrier D(2021)Clinical characteristics of 1,055 Chinese patients with Mayer–Rokitansky–Küster–Hauser syndrome: a nationwide multicentric study Fertil Steril 116 558-368

[7] Bjørsum-Meyer T(2016)Prevalence and patient characteristics of Mayer–Rokitansky–Küster–Hauser syndrome: a nationwide registry-based study Hum Reprod 31 2384-1267

[8] Herlin M(2015)Typical and atypical associated findings in a group of 346 patients with Mayer–Rokitansky–Kuester–Hauser Syndrome J Pediatr Adolesc Gynecol 28 362-576

[9] Qvist N(2009)Rectovestibular fistula—rarely recognized associated gynecologic anomalies J Pediatr Surg 44 1261-undefined

[10] Petersen MB(2012)Vaginal agenesis or distal vaginal atresia associated with anorectal malformations J Pediatr Surg 47 571-undefined

[1] Londra L(2015)Mayer–Rokitansky–Kuster–Hauser–syndrome: a review Int J Womens Health 2 865-870

[2] Chuong FS(2007)Mayer–Rokitansky–Küster–Hauser (MRKH) syndrome Orphanet J Rare Dis 14 13-458

[3] Kolp L(2016)Vertebral defect, anal atresia, cardiac defect, tracheoesophageal fistula/esophageal atresia, renal defect, and limb defect association with Mayer–Rokitansky–Küster–Hauser syndrome in co-occurrence: two case reports and a review of the literature J Med Case Rep 21 374-302

[4] Morcel K(2013)Investigation of the freely available easy-to-use software ‘EZR’ for medical statistics Bone Marrow Transplant 48 452-565

[5] Camborieux L(2003)Contemporary issues in primary amenorrhea Obstet Gynecol Clin 30 287-2390

[6] Guerrier D(2021)Clinical characteristics of 1,055 Chinese patients with Mayer–Rokitansky–Küster–Hauser syndrome: a nationwide multicentric study Fertil Steril 116 558-368

[7] Bjørsum-Meyer T(2016)Prevalence and patient characteristics of Mayer–Rokitansky–Küster–Hauser syndrome: a nationwide registry-based study Hum Reprod 31 2384-1267

[8] Herlin M(2015)Typical and atypical associated findings in a group of 346 patients with Mayer–Rokitansky–Kuester–Hauser Syndrome J Pediatr Adolesc Gynecol 28 362-576

[9] Qvist N(2009)Rectovestibular fistula—rarely recognized associated gynecologic anomalies J Pediatr Surg 44 1261-undefined

[10] Petersen MB(2012)Vaginal agenesis or distal vaginal atresia associated with anorectal malformations J Pediatr Surg 47 571-undefined