Results 121 to 130 of about 34,800 (289)

Anorectal prolapse after anorectal reconstruction: Incidence and risk factors according to the ARM‐Net Consortium

open access: yesColorectal Disease, Volume 27, Issue 2, February 2025.
Abstract Aim There is a knowledge gap regarding which patients with anorectal malformations (ARMs) are at highest risk of anorectal prolapse (AP), and which risk factors predispose to AP in ARM. The aims of the study were to define the frequency of AP after ARM reconstruction, and explore risk factors.
Pernilla Stenström   +10 more
wiley   +1 more source

Rectal diaphragm in a patient with imperforate anus and rectoprostatic fistula

open access: yesJournal of Indian Association of Pediatric Surgeons, 2009
The association of rectal diaphragm in an imperforate anus has not been reported until now. A 1-year-old male presented with right transverse colostomy for high anorectal malformation.
Thakur Ashokanand   +3 more
doaj  

Converting the ANU 2.3 telescope to fully automated operation [PDF]

open access: yesPublications of the Astronomical Society of Australia, Volume 41, article id. e057 (September 2024)
The operation of the ANU 2.3m telescope transitioned from classically scheduled remote observing to fully autonomous queue scheduled observing in March 2023. The instrument currently supported is WiFeS, a visible-light low-resolution image-slicing integral field spectrograph with a 25''x 38'' field of view (offering precision spectrophotometry free ...
arxiv   +1 more source

The Cosmic BPT Diagram: Confronting Theory with Observations [PDF]

open access: yes, 2013
We compare a large sample of galaxies between 0.51.5) are consistent with a model in which the ISM conditions are more extreme at high redshift than seen in the ...
arxiv   +1 more source

Anorectal malformations at University Teaching Hospital of Butare in Rwanda: A review of 46 operative cases [PDF]

open access: yes, 2016
Background: Anorectal malformations (ARM) are comprised of a wide spectrum of disease that involves congenital anomalies of the anus and rectum, as well as the urinary and genital tracts. They occur in approximately 1 in 5000 live births and affect males
Kakande, I, Makanga, M, Ntirenganya, F
core   +2 more sources

Goldenhar Syndrome and Surgical Reconstruction: A Case Report of Bilateral Complete Eyelid Colobomas in a 2‐Day‐Old Patient

open access: yesCase Reports in Ophthalmological Medicine, Volume 2025, Issue 1, 2025.
Goldenhar syndrome (GS), also known as Franceschetti–GS, encompasses a spectrum of congenital anomalies affecting the eyes, ears, face, and vertebrae. This case report highlights a 2‐day‐old female patient diagnosed with GS presenting a rare manifestation of bilateral complete eyelid colobomas.
Rawan S. Utt   +6 more
wiley   +1 more source

Omphalocele, exstrophy of cloaca, imperforate anus and spinal defect (OEIS Complex): A case report

open access: yes, 2015
Omphalocele, exstrophy of cloaca, imperforate anus and spinal defect (OEIS Complex) is an extremely rare combination of serious defects, which was firstlydescribed by Carey and colleagues. Surgical repair of cloacal exctrophy in patientswith OEIS complex
M. Kaya   +3 more
semanticscholar   +1 more source

A rare case of perineal hamartoma associated with cryptorchidism and imperforate anus: case report

open access: yesEinstein, 2014
A full-term male neonate with anorectal anomaly and external perineal anomalies was referred to our service. Physical examination showed an epithelized perineal mass with cutaneous orifices, which had urine fistulization, hipotrofic perineal musculature,
K. Yamaçake   +3 more
semanticscholar   +1 more source

Urinary Complications Among Patients With Anorectal Malformation Seen At Gezira National Center Of Pediatric Surgery-Sudan [PDF]

open access: yes, 2020
Background: Anorectal malformation (ARM) is a spectrum of structural congenital defects involving the anorectum and variable segments of the urogenital system in boys and girls, incidence occurs in 1 in 5000 births, The malformations range from skin ...
Nugud, Faisal, Yagoub, Adam
core   +1 more source

An inherited TBX3 alteration in a prenatal case of ulnar‐mammary syndrome: Clinical assessment and functional characterization in Drosophila melanogaster

open access: yesJournal of Cellular Physiology, Volume 239, Issue 12, December 2024.
Abstract Ulnar mammary syndrome (UMS) results from heterozygous variants in the TBX3 gene and impacts limb, tooth, hair, apocrine gland, and genitalia development. The expressivity of UMS is highly variable with no established genotype–phenotype correlations.
Irene Bottillo   +12 more
wiley   +1 more source

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