Results 91 to 100 of about 2,639 (226)

AMHR2 mutation in persistent Müllerian duct syndrome: A case of transverse testicular ectopia

UroPrecision, Volume 4, Issue 1, Page 64-68, March 2026.
Abstract Backgroud Persistent Müllerian duct syndrome (PMDS) is a rare condition characterized by the persistence of Müllerian duct structures in genotypic and phenotypic males. Case Presentation We present the case of a 4‐month‐old male with PMDS who presented with transverse testicular ectopia. The patient underwent diagnostic laparoscopic orchiopexy
Hangcheng Fu, Weijing Huang, Jeffrey T. White   +2 more
wiley   +1 more source

Anorectal malformation with didelphys uterus: Extremely rare anomaly and successful neoanal sphincter reconstruction with gracilis muscle flap

Archives of Plastic Surgery, 2020
Anorectal malformation or imperforate anus is a congenital anomaly of rectum and anus. Mullerian duct anomalies are abnormal development of uterus, cervix, and vagina.
Chairat Burusapat, Natthawoot Hongkarnjanakul, Nutthapong Wanichjaroen, Sakchai Panitwong, Jiraporn Sangkaewsuntisuk, Chinakrit Boonya-ussadorn   +5 more
doaj   +1 more source

Changes in the Mare Oviduct Across Different Seasons Throughout the Year

Veterinary Medicine and Science, Volume 12, Issue 2, March 2026.
Checking changes throughout the year in the oviductal structure (anatomy, permeability, oviductal cellularity and the presence of pathologies) may be relevant to understand the influence on the appearance of problems in oviductal functionality. The oviducts of 56 mares were examined, and the correlations between the time of the year and each of these ...
Noelia González, Agatha Varela, Nacho de Blas, Lydia Gil   +3 more
wiley   +1 more source

A rare case of OHVIRA (obstructed hemivagina and ipsilateral renal anomaly) syndrome: Case report

Radiology Case Reports
Obstructed hemivagina and ipsilateral renal anomaly syndrome (OHVIRA) also known as Herlyn-Werner-Wunderlich syndrome is a rare type of Müllerian duct anomaly with concomitant mesonephric duct anomalies.
Natnael Alemu Bezabih, Abdudin Heru Mehammed, Muluken Yifru Gebresilassie, Nebiyu Damtew Regasa   +3 more
doaj   +1 more source

Herlyn-Werner-Wunderlich syndrome presenting with infertility: Role of MRI in diagnosis

Indian Journal of Radiology and Imaging, 2013
Herlyn-Werner-Wunderlich syndrome (HWWS), characterized by uterus didelphys, obstructed hemivagina, and ipsilateral renal agenesis, is an uncommon combined Mullerian and mesonephric duct anomaly, and its presentation in adulthood is even rarer. We report
Zohra Ahmad, Ankur Goyal, Chandan J Das, Dipika Deka, Raju Sharma   +4 more
doaj   +1 more source

Analysis of Mullerian developmental defects in a tertiary care hospital: a four year experience [PDF]

, 2017
Background: Mullerian duct anomalies are congenital anomalies of the female genital tract. Mullerian duct anomalies affect the reproductive health of the female to a varied extent. This may present as obstructive or as non-obstructive anomalies.
Desai, Ajesh N., Modi, Komal P., Pamnani, Dirgha H., Patel, Swati N.   +3 more
core   +2 more sources

Unruptured ectopic pregnancy in rudimentary horn of unicornuate uterus at fourteen weeks with previous vaginal delivery [PDF]

, 2020
Unicornuate uterus with a rudimentary horn is an anomaly of the mullerian duct and is an extremely rare condition. This condition results when one of the paired mullerian ducts fails to fuse completely.
Hindocha, Jaydip, Sonaiya, Sneh
core   +2 more sources

Cutaneous Ciliated Cyst of the Ear

Pediatric Dermatology, Volume 43, Issue 2, Page 391-394, March/April 2026.
ABSTRACT Cutaneous ciliated cysts are rare benign lesions initially observed exclusively in the lower extremities of young females. Since their first descriptions, there have been numerous case reports of the entity occurring in males and females, in varying anatomical locations. Here, we present a case of cutaneous ciliated cyst reported for the first
Allan Fong, Andrew H. Huang, Jonathan Bush   +2 more
wiley   +1 more source

Transverse testicular ectopia with Müllerian duct remnant in an incarcerated congenital inguinal hernia – a case report

BMC Urology, 2020
Background Transverse testicular ectopia (TTE) is a rare anomaly characterized by both testes descending through a single inguinal canal. In this report, the diagnosis of TTE was discovered in the event of an incarcerated congenital inguinal hernia in a ...
Mostafa Kotb, Ahmed Hassan, Mohamed Abouheba   +2 more
doaj   +1 more source

Anatomical Variations, Genitourinary Anomalies and Clinical Presentations in Obstructed Hemivagina and Ipsilateral Renal Anomaly Syndrome: Case Series

Journal of the Korean Society of Radiology
Obstructed hemivagina and ipsilateral renal anomaly (OHVIRA) syndrome is a rare Müllerian duct anomaly, commonly characterized by uterus didelphys, obstructed hemivagina, and ipsilateral renal agenesis.
Hyun Jeong Kim, Eun Ji Lee, Yun-Woo Chang, Seong Sook Hong, Jiyoung Hwang, Boda Nam, Sung Hwan Bae   +6 more
doaj   +1 more source