Results 71 to 80 of about 739 (175)

Spectrum of Etiologies Causing Hydrometrocolpos

open access: yesJournal of Neonatal Surgery, 2013
Background: Hydrometrocolpos (HMC) develops as a result of vaginal outflow obstruction and the accumulation of secretions. It might be secondary to persistent cloaca, urogenital sinus, some syndromes, presence of the vaginal septum, vaginal atresia, and imperforate hymen. Each of them has different treatment options and follow-up protocols.
Aysenur, Cerrah Celayir   +3 more
openaire   +3 more sources

Anestesia em paciente portadora de síndrome de Mckusick-Kaufman: relato de caso Anestesia en paciente portadora de síndrome de Mckusick-Kaufman: relato de caso Anesthesia in Mckusick-Kaufman syndrome patient: case report

open access: yesRevista Brasileira de Anestesiologia, 2004
JUSTIFICATIVA E OBJETIVOS: A síndrome de Mckusick-Kaufman é uma doença rara, caracterizada tipicamente por hidrometrocolpos, polidactilia e defeitos cardíacos congênitos.
Adriano Bechara de Souza Hobaika   +2 more
doaj   +1 more source

Hydrometrocolpos, postaxial polydactyly, and hypothalamic hamartoma in a patient with confirmed Pallister-Hall syndrome: a clinical overlap with McKusick-Kaufman syndrome

open access: yes, 2008
We present a preterm-born girl with polydactyly of both hands and massive hydrometrocolpos, the latter due to vaginal atresia. This association led initially to the diagnosis of McKusick-Kaufman syndrome (MKKS).
Zeilinger, Georg   +9 more
core   +1 more source

The Mckusick-Kaufman syndrome: report of a case with some associations

open access: yesThe Turkish Journal of Pediatrics, 2002
McKusick-Kaufman syndrome (MKS) is a rare autosomal recessive condition consisting of congenital hydrometrocolpos, polydactyly and congenital heart defect.
Esin Kotiloğlu   +3 more
doaj  

Hydrometrocolpos, postaxial polydactyly, and hypothalamic hamartoma in a patient with confirmed Pallister-Hall syndrome: a clinical overlap with McKusick-Kaufman syndrome [PDF]

open access: yes, 2018
We present a preterm-born girl with polydactyly of both hands and massive hydrometrocolpos, the latter due to vaginal atresia. This association led initially to the diagnosis of McKusick-Kaufman syndrome (MKKS).
Zeilinger, Georg   +4 more
core  

A rare case of hydrometrocolpos from persistent urogenital sinus in patient affected by adrenogenital syndrome

open access: yes, 2018
Persistent urogenital sinus (PUGS) is a congenital pathological condition characterized by an abnormal communication between the urethra and vagina, which has an estimated incidence of 0.6/10,000 female births.
Maria Grazia Caprio   +16 more
core   +1 more source

Prenatal Diagnosis of Persistent Urogenital Sinus with Duplicated Hydrometrocolpos and Ascites – A Case Report

open access: yes, 2010
We report a successful case of persistent urogenital sinus associated with a duplicated nonsyndromic form of hydrometrocolpos and ascites diagnosed prenatally.
Juliette Dupont   +7 more
core   +1 more source

A rare case of pyometrocolpos with obstructive uropathy: sequelae of distal vaginal atresia

open access: yes, 2018
Hydrometrocolpos is a rare abnormality in female newborns. It follows congenital vaginal obstruction which may present as a midline abdominal mass causing either urinary tract or gastrointestinal tract obstruction without a coexisting bowel anomaly.
Ajayi, O.I., Balogun, B.O.
core   +1 more source

The neonatal management and surgical correction of urinary hydrometrocolpos caused by a persistent urogenital sinus

open access: yes, 1999
OBJECTIVE: To define the neonatal management and ultimate surgical correction via the anterior sagittal transanorectal approach (ASTRA) in cases of neonatal urinary hydrometrocolpos associated with a persistent urogenital sinus (UGS).
ROMEO, Carmelo   +5 more
core  

Abdominal Distention and Acute Urinary Retention secondary to Congenital Distal Vaginal Obstruction in a Newborn Female

open access: yesمجله كليه طب الكندي, 2009
Congenital distal vaginal obstruction is usually asymptomatic in a newborn female. On rare occasions, it may present as an acute emergency with life threatening complications.This paper is reporting the rare condition of two newborn females presenting ...
Nian Noori Ameen   +2 more
doaj  

Home - About - Disclaimer - Privacy