Results 41 to 50 of about 739 (175)
Early abdomino-perineal pull-through vaginoplasty
African Journal of Paediatric Surgery, 2013 Vaginal agenesis is known as one of the Mόllerian anomalies. Mόllerian anomalies occur during gonadal development and differentiation, and may lead to complex outcomes.
Ilhan Ciftci +3 more
doaj +1 more source
Hydrometrocolpos presenting as a huge abdominal swelling and obstructive uropathy in a 4 day old newborn: A diagnostic challenge [PDF]
, 2016 BACKGROUND: Abdominal swelling is an uncommon presentation in newborn babies. A combination of huge abdominal swelling, obstructive uropathy and imperforate hymen in newborns has not been reported in the medical literature.CASE DETAILS: We report a 4 ...
Tadele, Henok +3 more
core +1 more source
Neonatal Hydrometrocolpos Secondary to Imperforate Hymen in a Two-Month Old Girl [PDF]
National Radiology Journal of PakistanCongenital hydrometrocolpos is a rare disorder in infants characterized by an expansion of vaginal and uterine cavities with fluid accumulation. This case report describes a rare condition, hydrometrocolpos, caused by an imperforate hymen in a two-month-
Khalil Hussain +3 more
doaj +1 more source
Hydrometrocolpos Due to Persistent Urogenital Sinus Mimicking Neonatal Ascites [PDF]
, 2008 Objective: A urogenital sinus is a common channel into which both the urethra and genital tracts open. Occasionally there might be transverse obstructing membrane leading to hydrometrocolpos from either uterine secretions or urine.
Ghani, Imran +2 more
core +1 more source
American Journal of Diseases of Children, 1962 Hydrometrocolpos has been infrequently reported in the world literature. Its true incidence is certainly much greater than the 22 cases cited in this report. Recognition and appropriate management depend upon some knowledge of the entity and its associated manifestations.
R, SPENCER, D M, LEVY
openaire +5 more sources
Prenatal ultrasonography and postnatal follow-up of a case of McKusick-Kaufman syndrome
Taiwanese Journal of Obstetrics & Gynecology, 2014 Objective: McKusick-Kaufman syndrome (MKS) is a rare autosomal recessive syndrome characterized by hydrometrocolpos (HMC) and postaxial polydactyly (PAP).
Hsing-Fen Tsai +4 more
doaj +1 more source
A case of McKusick-Kaufman syndrome [PDF]
Korean Journal of Pediatrics, 2011 McKusick-Kaufman syndrome (MKS) is an autosomal recessive multiple malformation syndrome characterized by hydrometrocolpos (HMC) and postaxial polydactyly (PAP).
Se-Hyung Son +6 more
doaj +1 more source
Case Reports in Obstetrics and Gynecology, Volume 2019, Issue 1, 2019., 2019 Transverse vaginal septum (TVS) is a particularly rare vaginal anomaly, and diagnosis is often difficult in a genital examination. We herein present a case of perforated TVS for which successful diagnosis and treatment were achieved using a new technique referred to as saline infusion sonocolpography.
Ayumi Ono +9 more
wiley +1 more source
#151 : Partial Urorectal Septum Malformation Sequence
Fertility & Reproduction, 2023 Background and Aims: Cloacal malformations represent a wide range of defects and are considered one of the most challenging and interesting diseases. Occurrence is at 1 in 50,000 newborns and still with an unknown etiology.
Jennifer Clarize Braña +2 more
doaj +1 more source
Endometrial Carcinoma in a 26‐Year‐Old Patient with Bardet‐Biedl Syndrome
Case Reports in Obstetrics and Gynecology, Volume 2018, Issue 1, 2018., 2018 Background. Bardet‐Biedl Syndrome (BBS) is a rare genetic condition characterized by cognitive impairment, dysmorphism, central obesity, and diabetes mellitus, among other abnormalities. Although some of these characteristics are known independent risk factors for endometrial cancer and its precursors, the association between BBS and endometrial cancer
Olga Grechukhina +6 more
wiley +1 more source