Results 91 to 100 of about 1,042 (196)
Long‐term effects of surgically corrected menstrual outflow obstruction: A case–control study
International Journal of Gynecology &Obstetrics, Volume 165, Issue 1, Page 117-124, April 2024.Abstract Objective To enhance evidence‐based knowledge on long‐term sequalae in patients with surgically corrected obstructing Müllerian anomalies. Methods This long‐term case–control study included patients with menstrual outflow obstruction due to congenital anomalies of the uterus or vagina, who were at least 18 years old, and for whom 2 years had ...
Lisanne Martens +4 more
wiley +1 more source
A rare case of symptomatic hydrometrocolpos in a 5y old female
Urology Case Reports, 2021 Late presentation of symptomatic hydrometrocolpos is uncommon. We present a 5 years old continent girl with prenatally diagnosed multicystic dysplastic left kidney and late-onset of lower abdominal pain.
Hussam Nassar, Maya Horst, Rita Gobet
doaj +1 more source
Uterine Didelphys with Pregnancy and Obstructed Labor: Intrapartum Course Complicated by a Rare Uterine Anomaly [PDF]
, 2021 Mullerian duct anomalies (MDAs) are congenital anatomic abnormalities of the female genital tract that arise from nondevelopment or non-fusion of the mullerian ducts or failed resorption of the uterine septum, with a reported incidence of 0.1-10.0%. MDAs
HEMALATHA M SHETTI, SHASHIDHAR B
core +1 more source
Clinical Case Reports, Volume 12, Issue 3, March 2024.Key Clinical Message OHVIRA syndrome can be misdiagnosed due to its rarity, resulting in the need for more invasive interventions than vaginoscopy. Also, delayed diagnosis of OHVIRA syndrome can affect patient's quality of life by leading to chronic gynecological diseases such as endometriosis and pelvic inflammatory disease.
Ameneh Haghgoo +3 more
wiley +1 more source
Middle East Fertility Society Journal, 2011 Background: Uterine didelphys with obstructed hemivagina is an extremely rare condition. This diagnosis should be considered whenever an adolescent is presented with severe dysmenorrhea and progressive pelvic mass. Case: A 15-year-old girl presented with
Kamal M. Zahran +3 more
doaj +1 more source
Case Reports in Radiology, Volume 2024, Issue 1, 2024.The Herlyn‐Werner‐Wunderlich syndrome (HWWS) is a very rare congenital anomaly of the urogenital tract. It is characterized by a combination of didelphys uterus, unilateral vaginal obstruction, and ipsilateral renal agenesis. MRI imaging is usually used for diagnosis; however, the authors present a case of HWWS diagnosed by ultrasonography (HSG) and ...
Hidayatullah Hamidi +2 more
wiley +1 more source
Hereditary neuropathy with liability to pressure palsies as a possible predisposing factor to the development of Chronic inflammatory demyelinating polyneuropathy [PDF]
, 2023 Chronic inflammatory demyelinating polyneuropathy (CIDP) is a symmetric distal muscle weakness and sensory deficit accompanied with diminished or absent deep tendon reflexes. Hereditary neuropathy with liability to pressure palsies (HNPP) is a hereditary
Bilić, Hrvoje +4 more
core +2 more sources
Uterine didelphus with obstructed hemivagina.
Saudi medical journal, 2008 Complex congenital anomalies of the mullerian ducts can occur in isolation or in association with other developmental disorders. They result from non-development or non-fusion of the mullerian ducts or the failure of reabsorption of the uterine septum.
Malak M, Al-Hakeem +3 more
openaire +1 more source
International Journal of Advanced Medical and Health Research, 2016 Obstructed hemivagina and ipsilateral renal anomaly syndrome is a rare group of urogenital anomalies in which unilateral genital anomaly is associated with ipsilateral renal anomaly.
Kapish Mittal +5 more
doaj +1 more source
Obstructive mullerian anamolies: a case series [PDF]
, 2019 AIM of the study was to review the heterogeneous clinical presentations and management options for some of the obstructive mullerian anomalies through a case series.
Kadam, V. K. +3 more
core +2 more sources