| Literature DB >> 34899045 |
Peter Oppelt1, Helge Binder1, Jacques Birraux2, Sara Brucker3, Irene Dingeldein4, Ruth Draths5, Felicitas Eckoldt6, Ulrich Füllers7, Olaf Hiort8, Dorit Hoffmann9, Markus Hoopmann3, Jürgen Hucke10, Matthias Korell11, Maritta Kühnert12, Barbara Ludwikowski13, Hans-Joachim Mentzel14, Dan Mon OʼDey15, Katharina Rall3, Michael Riccabona16, Stefan Rimbach17, Norbert Schäffeler18, Sandra Shavit19, Raimund Stein20, Boris Utsch21, Rene Wenzl22, Peter Wieacker23, Mazen Zeino24.
Abstract
Objectives Female genital malformations may take the form of individual entities, they may involve neighboring organs or they may occur in the context of complex syndromes. Given the anatomical structures of the vulva, vagina, uterus and adnexa, the clinical picture of malformations may vary greatly. Depending on the extent of the malformation, organs of the urinary system or associated malformations may also be involved. Methods This S2k-guideline was developed by representative members from different medical specialties and professions as part of the guidelines program of the DGGG, SGGG and OEGGG. The recommendations and statements were developed using a structured consensus process with neutral moderation and voted on. Recommendations The guideline is the first comprehensive presentation of the symptoms, diagnosis and treatment options for female genital malformations. Additional chapters on classifications and transition were included. Thieme. All rights reserved.Entities:
Keywords: MRKH; bladder exstrophy; cloacal malformation; genital malformation; genital reconstruction; guideline; subseptate uterus; vaginal septum
Year: 2021 PMID: 34899045 PMCID: PMC8654513 DOI: 10.1055/a-1471-4781
Source DB: PubMed Journal: Geburtshilfe Frauenheilkd ISSN: 0016-5751 Impact factor: 2.915