Results 61 to 70 of about 1,400,939 (196)

Management of congenital female genital tract anomalies related to primary amenorrhea and/or cyclic abdominal pain: A retrospective cohort study

Acta Obstetricia et Gynecologica Scandinavica, Volume 105, Issue 9, Page 1810-1822, September 2026.
Overall, 21 patients with uterine, cervical, and vaginal aplasia were treated successfully with neovagina formation. In 6 out of 8 patients, with obstructed uterine cavity, anastomosis was successful; one underwent hysterectomy and one elective hemi‐hysterectomy.
Grigoris F. Grimbizis, Sofia Tsiapakidou, Eirini Iordanidou, Georgios Kioussis, Anastasia Vatopoulou, Theodoros Theodoridis   +5 more
wiley   +1 more source

Single‐Stage Uterovaginal Anastomosis: A Surgical Solution for Primary Amenorrhea Due to Vaginal Agenesis: A Case Series

Clinical Case Reports, Volume 14, Issue 8, August 2026.
ABSTRACT Here we present follow up of 3 cases of mid vaginal atresia and a functional uterus treated by single stage utero vaginal anastomosis using rectal tube insertion in uterus (for drainage) simultaneously with the amnion graft for vaginoplasty. This procedure successfully restored regular menstruation with fertility preservation and low morbidity.
Elham Askary, Zahra Parsaiyan, Nahideh Afshar Zakaria, Saeed Alborzi, Tahereh Poordast, Shaghayegh Moradi Alamdarlo   +5 more
wiley   +1 more source

Modern competency‐based teaching of human sexual development

Anatomical Sciences Education, Volume 19, Issue 7, Page 1086-1096, July 2026.
Abstract Embryology is an integral part of anatomy and a key subject in basic medical education. The development of the sexual tract, which is closely associated with the formation of the urinary tract and the organs of continence, is particularly complex and relevant for many medical disciplines.
Elisabeth Eppler, Alessandro Bilella, Christian M. Hammer   +2 more
wiley   +1 more source

Müllerian Agenesis Presenting as Primary Amenorrhea in a 16‐Year‐Old Girl From a Low‐Resource Setting in Bangladesh: Psychological Impact and Multidisciplinary Management

Clinical Case Reports, Volume 14, Issue 7, July 2026.
ABSTRACT Müllerian agenesis (MRKH syndrome) causes primary amenorrhea in phenotypically normal females. We report a 16‐year‐old girl with normal secondary sexual characteristics, a short blind vagina, absent uterus on ultrasonography, and a 46,XX karyotype.
Iftekhar Ahmed Sakib, Musarrat Sultana Shumi, Rozina Sultana, Ayesa Perveen, Nishad Tasnim, Shirazum Munira   +5 more
wiley   +1 more source

ISOLATED MAYER-ROKITANSKY-KUSTER-HAUSER (MRKH) SYNDROME: A CASE REPORT AND REVIEW OF THE LITERATURE.

, 2018
Introduction: Mayer-Rokitansky-Kuster-Hauser (MRKH) syndrome is a congenital disorder of unknown etiology, characterized by mullerian agenesis and can be associated with renal, skeletal and cardiac malformation. Most cases are sporadic. Case Report: We
*Dr. Abiha Ahmad Khan, Prof. S. A. Naaz, Prof. Wajeeha Begum
core   +1 more source

A Case of Iron Overload–Associated Hypogonadism and Mayer–Rokitansky–Küster–Hauser Syndrome in a Patient With Thalassemia

Annals of Internal Medicine: Clinical Cases
We report a rare case of a 22-year-old woman with transfusion-dependent beta-thalassemia major who presented with primary amenorrhea. Work-up revealed dual etiologies: hypogonadotropic hypogonadism attributable to pituitary iron overload and müllerian ...
Ravi Krishnegowda, Nagaraja Kamath, Naveen Kumar, Rishika Das, Aditya Chandrashekar   +4 more
doaj   +1 more source

Chronic kidney disease in Mayer-Rokitansky-Kuster-Hauser Syndrome

Indian Journal of Nephrology, 2010
Mayer-Rokitansky-Kuster-Hauser (MRKH) syndrome is characterized by either absence or abnormalities of the mullerian structures. It is a rare disorder, resulting in complete or partial agenesis of the uterus and cervix and primary amenorrhea. It may rarely be associated with anomalies of the urinary tract, ovaries and skeleton.
Wani, M. M., Mir, S. A.
openaire   +2 more sources

Genetic Characterization and Multidisciplinary Management of Complete Androgen Insensitivity Syndrome: Unveiling a Novel AR Mutation

Clinical Case Reports, Volume 14, Issue 5, May 2026.
ABSTRACT A novel AR frameshift mutation (c.2023_2035del) was identified in a 17‐year‐old phenotypic female with Complete Androgen Insensitivity Syndrome (CAIS). This report emphasizes the necessity of molecular characterization and multidisciplinary management to address diagnosis, surgical timing, and psychological well‐being in disorder of sex ...
Maria Francesca Astorino, Serena Scalise, Chiara Di Bella, Maria Angela La Rosa, Basilia Piraino, Marco Calabrò, Mattia Gentile, Rosaria Maddalena Ruggeri, Emanuela Esposito, Silvana Briuglia, Salvatore Cannavò   +10 more
wiley   +1 more source

Mayer Rokitansky Kuster Hauser syndrome: A case of Mullerian Agenesis

, 2021
Developmental anomalies of the Mullerian duct are one of the fascinating congenital disorders encountered in which Mayer Rokitansky Kuster Hauser syndrome (MRKH) is one of the wide variety of malformations.
Baby, Anu, Kurian, Simi, Jose, Rani
core  

Paraparesis and congenital severe hyperkyphosis in Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome: A rare deformity management during the Sars-Cov-2 pandemic

Brain and Spine, 2023
Introduction: Mayer-Rokitansky-Küster-Hauser syndrome (MRKH) syndrome can be classified into two types: type I (isolated) without extragenital abnormalities; type II (associated) with the presence of extragenital dimorphisms.
Giovanni Andrea La Maida, Andrea Della Valle, Enrico Gallazzi, Marcello Ferraro, Davide Cecconi, Alfonso Cicatelli, Daniele Priano, Luca La Verde, Bernardo Misaggi   +8 more
doaj   +1 more source