Results 11 to 20 of about 2,297 (217)
Diagnostic difficulties in a case of persistent cloaca with hydrocolpos. [PDF]
J Neonatal Surg, 2012 Pelvic midline cystic mass associated with renal malformation represents typical imaging features of a cloacal anomaly. We report a case of persistent cloaca that was diagnosed antenatally with fetal ultrasonography and MRI.
Sahinoglu Z +3 more
europepmc +4 more sources
Prenatal diagnosis of persistent cloaca
Congenital Anomalies (discontinued), 2009 ABSTRACTWe report four cases of persistent cloaca diagnosed at 32–33 weeks of gestation. In cases of persistent cloaca, serial prenatal ultrasonography shows transient fetal ascites, enlarged cystic structures arising from the fetal pelvis. Our four cases of persistent cloaca were diagnosed prenatally.
Nobuhiro Suzumori
exaly +4 more sources
The current profile of persistent cloaca and cloacal exstrophy in Japan: the results of a nationwide survey in 2014 and a review of the literature [PDF]
Pediatric Surgery International, 2017 Masayuki Kubota, Kubota Masayuki
exaly +2 more sources
Persistent cloaca: persistence of the challenge [PDF]
Annals of Pediatric Surgery, 2020 Abstract Background Persistent cloaca or cloacal anomalies represent a special category of anorectal anomalies affecting the female sex with a reported incidence of about one in 25,000 live birth. The study included 34 cases of cloaca that were managed at our unit between 2003 through 2017.
Amr Abdelhamid AbouZeid +3 more
openaire +1 more source
Treatment strategies for OIES complex/cloacal extrophy
Journal of Pediatric Surgery Case Reports, 2021 Cloacal exstrophy is the rarest and most severe form of the exstrophy epispadias complex. Before the 1960s the multiple systemic defects found in association with this anomaly in most cases lead to death of the infant. Developments in surgical technology,
Aqeela J. Madan, Saeed Alhindi
doaj +1 more source
A Unique Case with Tracheal Atresia Among Published Literature on TACRD and VACTERL Associations
Journal of Behçet Uz Children's Hospital, 2023 Tracheal atresia/agenesis (TA) is associated with other congenital anomalies (TACRD and/or VACTERL). In this study, a female newborn with TA who had all the elements associated with TACRD and VACTERL was reported.
Sabri Cansaran +3 more
doaj +1 more source
Journal of Diagnostic Medical Sonography, 2001 Hydrometrocolpos is a rare congenital disorder in which excessive mucus secretions accumulate from a genital tract obstruction resulting in cystic dilatation of the vagina and uterus. The spectrum of hydrometrocolpos is broad, ranging from mild cases undetected until adolescence to more severe conditions described prenatally as a large pelviabdominal ...
Steven R. Baier +2 more
openaire +1 more source
Next-generation sequencing identifies the Danforth's short tail mouse mutation as a retrotransposon insertion affecting Ptf1a expression. [PDF]
PLoS Genetics, 2013 The semidominant Danforth's short tail (Sd) mutation arose spontaneously in the 1920s. The homozygous Sd phenotype includes severe malformations of the axial skeleton with an absent tail, kidney agenesis, anal atresia, and persistent cloaca.
Christopher N Vlangos +6 more
doaj +1 more source
Global Pediatrics, 2023 Backgrounds: In persistent cloaca (PC), the vagina, urethra, and rectum are fused together in the pelvis, creating a common channel (CC). CC length, short or long will determine the definitive surgery and can be evaluated preoperatively using ...
Emiliana Lia +2 more
doaj +1 more source
Challenges in the Prenatal Diagnosis of Cloaca
Global Pediatric Health, 2020 Background: Cloaca is a common excretory channel for the genital, urinary, and gastrointestinal tracts. It is considered a severe anorectal malformation caused by failed partitioning of the genital, rectal, and urinary tracts.
Lisa B.E. Shields MD +3 more
doaj +1 more source