Results 91 to 100 of about 931 (167)

A rare case of Herlyn-Werner-Wunderlich syndrome-with pregnancy

open access: yesThe Egyptian Journal of Radiology and Nuclear Medicine, 2016
Herlyn-Werner-Wunderlich syndrome also known as uterus didelphys with obstructing hemivaginal septum and ipsilateral renal agenesis (OHVIRA) is a very rare syndrome with only a few case reported.
Vikas Deswal   +3 more
doaj   +1 more source

A Case Report on Ohvira Syndrome

open access: yesINTERANTIONAL JOURNAL OF SCIENTIFIC RESEARCH IN ENGINEERING AND MANAGEMENT
A 24 years old nullipara women was admitted in gynaecological ward with a history of whitish vaginal discharge for 6 months. On assessment her BP was 120/70 mm hg ,and she was conscious and oriented. Then she undergone investigations like USG and confirmed OHIVRA SYNDROME.
Dr.Sreerenjini B, Ms Kanimozhi
openaire   +1 more source

Herlyn-Werner-Wunderlich syndrome: A rare cause of abdominal pain and dyspareunia

open access: yesRadiology Case Reports, 2019
Herlyn-Werner-Wunderlich (HWW) syndrome is a rare congenital disease characterized by Mullerian duct anomalies. The characteristic triad of this syndrome includes didelphys uterus, obstructed hemivagina, and ipsilateral renal agenesis (hence, also known ...
Ninad Salastekar, MBBS, MPH   +3 more
doaj   +1 more source

A rare case report of urogenital anomaly in a teenage girl: Herlyn–Werner–Wunderlich syndrome/OHVIRA syndrome (Obstructed Hemivagina and Ipsilateral Renal Anomaly)

open access: yesThe Egyptian Journal of Radiology and Nuclear Medicine
Background Herlyn–Werner–Wunderlich syndrome also known as OHVIRA syndrome is a rare complex congenital developmental anomaly characterized by the triad of uterine didelphys, obstructed hemivagina causing hematometrocolpos and ipsilateral renal anomaly ...
Govardhana Das Joel   +2 more
doaj   +1 more source

Herlyn-Werner-Wunderlich syndrome complicated with pyocolpos: an unusual cause of postabortal sepsis [PDF]

open access: yes, 2016
Obstructive mullerian anomalies give rise to a spectrum of clinical presentations and are uncommon in routine gynecologic practice. The patient usually becomes symptomatic in early reproductive years.
Gaikwad, Ramesh   +3 more
core   +1 more source

Müllerian anomalies and endometriosis as potential explanatory models for the retrograde menstruation/implantation and the embryonic remnants/celomic metaplasia pathogenic theories: a systematic review and meta-analysis [PDF]

open access: yes
Study question: Does endometriosis prevalence differ in patients with obstructive Müllerian anomalies (OMA) versus those with nonobstructive Müllerian anomalies (NOMA), and in patients with NOMA versus those without Müllerian anomalies? Summary answer:
Edgardo Somigliana   +6 more
core   +1 more source

An Unusual Case of Recurrent Pyocolpos Following Midtrimester Miscarriage Revealed as Obstructed Hemivagina with Ipsilateral Renal Agenesis (OHVIRA) Syndrome

open access: yesOnline Journal of Health & Allied Sciences, 2014
Obstructed hemivagina with ipsilateral renal agenesis (OHVIRA Syndrome) is a rare congenital anomaly. It mostly presents with severe dysmenorrhea and a palpable mass due to unilateral hematocolpos.
Haldar M   +5 more
doaj  

思春期の下腹部痛を主訴に受診したOHVIRA症候群 (obstructive hemivagina and ipsilateral renal anomaly syndrome)の 3 例 [PDF]

open access: yes, 2021
OHVIRA症候群(obstructive hemivagina and ipsilateral renal anomaly syndrome)は重複子宮膣と片側膣閉鎖,患側腎欠損を合併する稀な疾患である.Wolff管の発生異常により,Müller管の癒合と腎形成に異常を来たすと考えられている.一般人口では 2 万人に 1 人にみられる.症例 1 は13歳,女児.下腹部痛があり,急性虫垂炎を疑われて紹介受診した.症例 2 は13歳,女児.右多嚢胞性異形性腎と膀胱尿管逆流の既往があった.右下腹部痛があり ...
中村 智子   +4 more
core   +1 more source

Case Series of Reproductive Outcomes after Surgical Correction of Obstructed Hemivagina in OHVIRA

open access: yesAmerican Journal of Perinatology Reports
Obstructed hemivagina and ipsilateral renal anomaly (OHVIRA) is a rare congenital developmental syndrome manifested by uterine duplication, lower genital tract obstruction, and unilateral renal anomaly. Literature on reproductive outcomes in this patient
Megan E. Bunnell   +2 more
doaj   +1 more source

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