Results 111 to 120 of about 277,660 (218)
Dilemma in diagnosis of pregnancy in didelphys uterus: a original case report [PDF]
Uterine didelphys is a congenital defect of female genital system that arises from abnormal embryological development of mullerian ducts. A 30-year-old female G4P3L3A0 at 9 weeks POG with uneventful previous three normal term delivery presented to gynae ...
Dogra, Kusum +2 more
core +2 more sources
Uterine Didelphys with Pregnancy Outcomes: A Case Report
Chattagram Maa-O-Shishu Hospital Medical College Journal, 2019 A didelphys uterus also known as a “double uterus” is one of the least common Mullerian duct anomalies. Uterine didelphys is a congenital malformation that result from complete failure of fusion of the ipsilateral Mullerian duct during embryonic development. Ideally, diagnosis should be made before pregnancy and labour to prevent adverse outcomes. Here
Farzana Rahman +2 more
openaire +2 more sources
Uterus transplantation: an experimental study in the rat model [PDF]
, 2012 One of the last frontiers to conquer in infertility research is to find a treatment for uterine factor infertility, which affects around 2500 Swedish women. These women cannot become pregnant or carry a pregnancy due to absence of uterus or presence of
Akhi, Musammad Shamima Nazmin
core
Prenatal Diagnosis, Volume 44, Issue 13, Page 1647-1658, December 2024.ABSTRACT Purpose MYRF‐related cardiac‐urogenital syndrome (MYRF‐CUGS) is a rare condition associated with heterozygous MYRF variants. The description of MYRF‐CUGS phenotype is mostly based on postnatal cases and 36 affected individuals have been published so far.
Maud Favier +34 more
wiley +1 more source
Notes on Marsupialian anatomy II. on the female genital organs of a virgin sarcophilus satanicus. [PDF]
, 1911 In a former communication to the Linnean Society of N.S.W. I described the genital apparatus in a female specimen of Sarcophilus satanicus which had borne young, and in that paper drew attention to various phenomena, especially in connection with the
Flynn, Theodore Thomson
core
Expansion of the core features of VACTERL association to include genital anomalies
American Journal of Medical Genetics Part A, Volume 194, Issue 9, September 2024.Abstract Genital anomalies have been reported with VACTERL association but not considered a core feature. Acute and chronic complications stemming from unrecognized genital anomalies have been reported in adolescents and young adults with VACTERL association. We sought to determine the frequency and severity of genital anomalies in VACTERL patients and
Laura T. Forero +4 more
wiley +1 more source
WNT4 deficiency—a clinical phenotype distinct from the classic Mayer-Rokitansky-Kuster-Hauser syndrome: A Case Report [PDF]
, 2017 The pathways leading to female sexual determination in mammals are incompletely defined. Loss-of-function mutations in the WNT4 gene appear to cause developmental abnormalities of sexual differentiation in women and mice.
Biason-Lauber, A. +5 more
core
Pregnancy in uterus didelphys delivered by caesarean section: a case report [PDF]
, 2017 The aim of this study is to report a rare case of pregnancy in uterus didelphys. Mullerian duct anomalies are congenital defects of the female genital system that arise from abnormal embryological development of the Mullerian ducts.
Sawai, Devashish Singh +5 more
core +2 more sources
Total laparoscopic hysterectomy with uterine didelphys [PDF]
American Journal of Obstetrics and Gynecology, 2022 P.L. Rosenblatt, H.M. French, S.A. Ward
openaire +1 more source
Obstructed hemivagina with ipsilateral renal agenesis (OHVIRA) syndrome with imperforate anus
Journal of Pediatric Surgery Case Reports, 2016 OHVIRA syndrome (Obstructed hemivagina with ipsilateral renal agenesis) is a rare Mullerian duct anomaly that results in uterine didelphys, obstructed vaginal vault, and unilateral renal agenesis.
Peter Cosgrove +3 more
doaj +1 more source