نتایج جستجو برای: mullerian anomaly

تعداد نتایج: 41271  

2012
Abdulrahim Gari Bandr Hafidh Adnan Gelidan Salah Kary Mazen Jan Hussein T. Sabban

Background: Vaginal agenesis is characterized by the absence or hypoplasia of the uterus, proximal vagina and the fallopian tubes. This anomaly has been recently termed müllerian aplasia by the American College of Obstetricians and Gynecologist. Müllerian aplasia is an uncommon, but not rare, anomaly. The estimated incidence is 1 in 5000 newborn females. Case: A 25 years old divorced female pre...

2016
Emel Unal Hikmet Gulsah Tanyildiz Murat Sonmezer Hatice Gul Erkol Suat Fitoz

Herlyn-Werner-Wunderlich (HWW) syndrome is a rare developmental anomaly that includes uterus didelphys with obstructed hemivagina and ipsilateral renal agenesis. A 13-year-old girl presented with chronic abdominal pain. Magnetic resonance imaging revealed uterus didelphys, hematometrocolpos and renal agenesis on the right side with imperforate hymen. Subsequently the patient was found to have M...

2015
Deepak Sharma Srinivas Murki Oleti Tejo Pratap GM Irfan Geeta Kolar

Neonatal hydrometrocolpos (HMC) is a rare Mullerian duct anomaly with an incidence of 0.006%. It occurs due to blockage of the vagina with accumulation of mucus secretions proximal to the obstacle. These secretions are secondary to intrauterine and postnatal stimulation of uterine and cervical glands by maternal estrogens. A triad of congenital HMC, polydactyly, and cardiac anomalies are the ca...

2005
Rusen Atmaca Aysegul Tezcan Germen Feza Burak Ayse Kafkasli

Unicornuate uterus with a rudimentary horn is the rarest congenital anatomic anomaly of the female genital system, causing many obstetrical and gynecologic complications. The frequency of this pathology is approximately 1/100 000. A rudimentary horn usually develops following insufficient development of mullerian ducts. These patients present with dysmenorrhea, dyspareunia, and chronic pelvic p...

2017
Shubhi Bhatnagar Shahaji Chavan Mahendra Bendre

INTRODUCTION Transverse aberrant testicular maldescent is an extremely rare congenital anomaly characterized by the migration of one testicle towards the opposite inguinal canal. Mostly such cases are reported in children and they are very rarely seen in adults. PRESENTATION OF CASE We report a case of a 24year old male patient with left reducible indirect inguinal hernia with absence of test...

2015
Mariya Angelova Angelova Emil Georgiev Kovachev Stefan Vasilev Kisyov Vilislava Robert Ivanova

The authors describe a case of a congenital Mullerian anomaly, uterus unicornis with missing right fallopian tube. An in Vitro Fertilization Pre-Embryo Transfer (IVF-ET) procedure was done and presently is known that the patient has left fallopian tube and left ovary, two kidneys, and right ovary is missing. No diagnostic laparoscopy and hysteroscopy were done, only hysterosalpingography (HSG) ...

2013
Kishor Taori Jawahar Rathod Ramesh Parate Amit Disawal Suresh Dhakate Anand Hatgaonkar Amrita Guha

The MURCS association which stands for Mullerian, Renal, Cervicothoracic Somite Abnormalities is a rare developmental anomaly seen in females. The clinical course of this disorder is not clearly defined as of yet-which may range from asymptomatic to severe disability. Here we present the case of a young 22-year-old female who was incidentally detected to have a generalized increase in bone dens...

Journal: :International journal of reproduction, contraception, obstetrics and gynecology 2022

Obstructed hemivagina and ipsilateral renal anomaly (OHVIRA) syndrome is a characterised by obstructed hemivagina, agenesis uterine didelphys. It rare congenital results from defective fusion of the Müllerian ducts during development female reproductive system. also known as Herlyn-Werner-Wunderlich syndrome. Aim study was to project case developmental Mullerian OHVIRA anomaly. The most common ...

Journal: :International Journal of Reproduction, Contraception, Obstetrics and Gynecology 2020

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