Results 61 to 70 of about 990 (163)
HERLYN WERNER WUNDERLICH SYNDROME;
Mullerian duct anomalies are underreported because these remain unrecognized. Unfortunately our knowledge of epidemiology has not paralleled the technical advances involved in their diagnosis and management. We report a case of 13 years old girl who presented with normal menarche and progressively severe dysmenorrhea. She was diagnosed to have a pelvic
openaire +3 more sources
Herlyn-Werner-Wunderlich Syndrome: Case Report [PDF]
Herlyn-Werner-Wunderlich sendromu (HWWS), Müllerian kanal anomalilerinin nadir görülen bir varyantıdır. Klasik triadı: kör hemivajina, uterin didelfis ve ipsilateral renal agenezidir. Klinik prezentasyonu genellikle menarş ile başlayan, progresif olarak artan ve hematokolposa sekonder gelişen şiddetli dismenoredir.
Taşkın, Mine İslimye +3 more
openaire +2 more sources
The Herlyn-Werner-Wunderlich (HWW) syndrome– A rare case report [PDF]
A 20-year-old unmarried female, student by occupation, well built and nourished presented with intermenstrual spotting from past 1 month. No h/o pelvic pain/ mass/ fever. No h/o of similar complaints in the past. Attained menarche at 14 years.
H L, Dr Harisha, Dr +2 more
core +1 more source
Herlyn-Werner-Wunderlich Syndrome: A Mini-review [PDF]
Herlyn-Werner-Wunderlich (HWW) syndrome is a rare congenital malformation syndrome that is characterized by a triad of uterine didelphys, blind hemivagina, and ipsilateral renal agenesis.
Jiwon M. Lee
doaj +1 more source
ABSTRACT Uterine didelphys, also known as double uterus, is a congenital anomaly of the female reproductive system that can be associated with a significant number of threatening obstetric complications, such as uterine rupture. We report a rare and complex case of an 18‐year‐old primigravida who presented with uterine rupture due to uterine didelphys ...
Asim Ali +7 more
wiley +1 more source
Magnetic resonance imaging in obstructive Müllerian anomalies
Herlyn-Werner-Wunderlich (HWW) syndrome is a very rare congenital anomaly of the urogenital tract involving Müllerian ducts and Wolffian structures.
Kamal Kumar Sen +2 more
doaj +1 more source
Paroxysmal nocturnal hemoglobinuria can rarely present as cerebral ischemia and stroke due to arterial thrombosis. However, it should be considered in a young patient with bone marrow failure features, systemic thromboses, and hemolysis.
Ayushma Acharya +3 more
doaj +1 more source
HERLYN-WERNER-WUNDERLICH SYNDROME-ROLE OF IMAGING IN TIMELY AND CORRECT DIAGNOSIS
We present this case of uterus didelphys with right sided haematometrocolpos due to obstructed hemivagina and ipsilateral renal agenesis-Herlyn Werner Wunderlich syndrome.
Hidayat Ullah +3 more
doaj +1 more source
Pregnancy in rudimentary horn of unicornuate uterus: a rare case [PDF]
Congenital malformations of the female genital tract result from embryological maldevelopment of Mullerian or paramesonephric ducts. Mullerian duct anomalies (MDAs) are due to agenesis, defective fusion or resorption during embryological development ...
Barkase, Akanksha A. +5 more
core +2 more sources
The Genetic Landscape of Müllerian Duct Anomalies: A Comprehensive Review
ABSTRACT Background Müllerian duct anomalies (MDAs) are developmental malformations of the female genital tract that present as a series of abnormalities within the reproductive tracts of females. The etiology of MDAs is complex and heterogeneous, especially genetic factors.
Lin He +6 more
wiley +1 more source

