Results 51 to 60 of about 5,455 (207)

Rare Associations with Posterior Urethral Valves

Case Reports in Urology, 2021
Posterior urethral valves are a common cause of congenital bladder outlet obstruction. Known associations include cardiac malformations and gastrointestinal abnormalities.
Ahmed Osama Mohamed, Bala Eradi, Anthony Owen, Ashok Rajimwale   +3 more
doaj   +1 more source

Cloacal Malformation with Associated Urethral Atresia

European Journal of Pediatric Surgery Reports, 2023
Introduction Cloacal malformations comprise a heterogeneous group of anomalies that are considered the most complex anorectal malformations (ARMs) in females.
Al-Shamaileh Al-Shamaileh, Tiusaba Tiusaba, Jacobs Jacobs, Russell Russell, Bokova Bokova, Pohl Pohl, Varda Varda, Ho Ho, Feng Feng, Badillo Badillo, Levitt Levitt   +10 more
doaj   +1 more source

Management of congenital female genital tract anomalies related to primary amenorrhea and/or cyclic abdominal pain: A retrospective cohort study

Acta Obstetricia et Gynecologica Scandinavica, EarlyView.
Overall, 21 patients with uterine, cervical, and vaginal aplasia were treated successfully with neovagina formation. In 6 out of 8 patients, with obstructed uterine cavity, anastomosis was successful; one underwent hysterectomy and one elective hemi‐hysterectomy.
Grigoris F. Grimbizis, Sofia Tsiapakidou, Eirini Iordanidou, Georgios Kioussis, Anastasia Vatopoulou, Theodoros Theodoridis   +5 more
wiley   +1 more source

Concurrent validity and agreement of Bayley‐4, AIMS, and HINE assessments in 1‐year‐old children

Developmental Medicine &Child Neurology, EarlyView.
In this cross‐sectional study of children around 1‐year‐old, the Bayley‐4 showed concurrent validity and moderate to substantial agreement with the AIMS and the HINE in both clinical and home settings. Abstract Aim To examine concurrent validity between the Bayley Scales of Infant and Toddler Development, Fourth Edition (Bayley‐4) gross motor subtest ...
Weiyang Deng, Bahda Hoang, Meaghan Rubsam, Gabriela Lopez, Megan K. O'Brien, Theresa Sukal‐Moulton, Barbara Sargent, Colleen Peyton, Elizabeth Hoffman, Samuel Carey, Nicole Pouppirt, Raye‐Ann de Regnier, John A. Rogers, Richard L. Lieber, Arun Jayaraman   +14 more
wiley   +1 more source

Birth prevalence of anorectal malformations in England and 5-year survival: a national birth cohort study [PDF]

, 2022
OBJECTIVE: To determine the birth prevalence, maternal risk factors and 5-year survival for isolated and complex anorectal malformations. DESIGN: National birth cohort using hospital admission data and death records.
Ford, Kathryn, Curry, Joe I, Peppa, Maria, Gilbert, Ruth, Zylbersztejn, Ania   +4 more
core  

Spontaneous bowel perforation in a neonate with anorectal malformation

The Saudi Journal of Gastroenterology, 2011
Gastrointestinal perforation in neonates with anorectal malformations is extremely uncommon. Delayed patient presentation is an important factor that demands special attention.
Gursev Sandlas, Paras Kothari, Dinesh Sarda, Parag Karkera   +3 more
doaj   +1 more source

Spatiotemporal remodelling of the cloacal region determines the position of the anal opening in mouse embryos

Journal of Anatomy, EarlyView.
In E13.25 mouse embryo, the urorectal septum consistently positioned on the dorsodistal side of the cloacal membrane. Through 3D reconstruction of the cloacal internal space, we revealed that the position of the anal opening is established prior to cloacal membrane rupture and is located at the junction between the hindgut lumen (blue) and an expanded ...
Weiyi Wang, Masayo Harada, Keiichi Akita
wiley   +1 more source

Segmental Infantile Hemangiomas That Involve the Midline Define Risk for LUMBAR Syndrome

Pediatric Dermatology, EarlyView.
ABSTRACT A systematic review of clinical photographs from 91 patients with LUMBAR syndrome demonstrated that infantile hemangiomas in affected individuals were consistently segmental in morphology and involved the anatomic midline of the lumbosacral, sacrococcygeal, or pelvic regions. No cases were “partial segmental” or spared the midline.
D. Metry, E. Fernandez‐Faith, A. Haggstrom, K. Keppler‐Noreuil, I. J. Frieden   +4 more
wiley   +1 more source

Dataset Exome chip association study in the etiology of anorectal malformations

, 2019
This dataset belongs to the publication "Exome chip association study excluded the involvement of rare coding variants with large effect sizes in the etiology of anorectal malformations", published in PLOS ONE in 2019 by van de Putte et al.
Rooij, dr. I.A.L.M. van (Radboud University) DAI=info:eu-repo/dai/nl/244772045, Putte, BSc R. van de (Radboud University), Roeleveld, dr. ir. N. (Radboud University) DAI=info:eu-repo/dai/nl/069298041, Reutter, H., Vermeulen, dr. H.H.M. (Radboud University) DAI=info:eu-repo/dai/nl/298981033, Kiemeney, prof. dr. L.A.L.M. (Radboud University) DAI=info:eu-repo/dai/nl/105132063, Wijers, dr. C.H.W. (Radboud University) DAI=info:eu-repo/dai/nl/329152211, Galesloot, dr. T.E. (Radboud University)   +7 more
core   +1 more source

Spontaneous ileal perforation complicating low anorectal malformation

African Journal of Paediatric Surgery, 2015
Anorectal malformation is a common anomaly in neonates. Although colorectal perforations have been reported as a complication, ileal perforation is rarely encountered.
TiJesuni Olatunji, Matthias Igoche, Pascal Anyanwu, Emmanuel A Ameh   +3 more
doaj   +1 more source