Results 81 to 90 of about 1,436 (213)
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
Cryptomenorrhea Secondary to Past Childhood Pelvic Trauma in Young Adolescent Girls: Case Series
Fertility & Reproduction, 2019 Primary amenorrhea secondary to childhood pelvic trauma is very rare. We report two cases of adolescent girls with cryptomenorrhoea. Case 1 presented at 14 years of age with primary amenorrhea and cyclical lower abdominal pain for 1 year.
Syeda Batool Mazhar +3 more
doaj +1 more source
Wunderlich--Herlyn--Werner syndrome [PDF]
, 2016 A 25 year old married and nulliparous woman with regular menstrual cycles presented with dyspareunia, infertility, increasing dysmenorrhea and recent onset vulval swelling in the gynaec outpatient department at Bhaskar medical college & Bhaskar ...
Biswas, Sathyakumar +4 more
core +2 more sources
Vaginoplasty and Fimbrioplasty on Vaginal Agenesis with Hematocolpos, Hematometra, and Hematosalpinx
Jurnal Kesehatan AndalasCongenital vaginal agenesis is a rare abnormality of the female genital tract caused by abnormal embryological development of the Müllerian ducts. Clinical manifestations vary depending on the extent of the anomaly, severity, and the patient's age at ...
Arnova Reswari +2 more
doaj +1 more source
OHVIRA syndrome and its incomplete variant: multimodality imaging insights from two distinct presentations of Müllerian-renal anomalies [PDF]
Mullerian anomalies such as obstructed hemivagina and ipsilateral renal anomaly (OHVIRA) syndrome pose diagnostic challenges due to their embryological variability and diverse clinical presentations.
B. S., Pavan, Pavuluri, Viharika
core +2 more sources
Hematocolpos and hematometra caused by imperforate hymen [PDF]
Medicinski Glasnik, 2007 Imperforate hymen is a rare congenital anomaly of the woman's reproductive system, with incidence of about 1/2000. The diagnosis is most frequently made during puberty after a menarche.
Đ. Ljuca +5 more
doaj
Imperforate hymen complicated by obstructive acute renal failure [PDF]
, 2012 Imperforate hymen is a rare malformation (1/ 1000 female births). It is diagnosed most often during puberty. Early diagnosis of hematocolpos and evacuation is necessary to avoid any consequences.
Diouf, M +5 more
core +2 more sources
Imperforate hymen presenting as acute urinary retention in an adolescent girl [PDF]
, 2016 Acute urinary retention in a female child is rare because of its anatomy. Haematocolpos can cause a mechanical obstruction, resulting in acute urinary retention.
Kumar, Santosh +2 more
core +2 more sources
Cryptomenorrhoea due to imperforate hymen: a case report [PDF]
, 2019 Imperforate hymen is a rare obstructive congenital anomaly of the female genital tract which arises as a result of complete failure of canalisation of the inferior end of the vaginal plate at the junction between the urogenital sinus and the vagina.
., Priyanka, ., Sneha, Bansal, Romi
core +2 more sources
Complete bicornuate uterus with complete transverse vaginal septum
Journal of Research in Medical Sciences, 2014 Bicornuate uterus has two symmetric uterine cavities that are fused caudally and have some degree of communication between two cavities, usually at the uterine isthmus. A complete bicornuate uterus has a seperatory cleft of tissue that is extended to the
Hatav Ghasemi Tehrani +2 more
doaj