Results 121 to 130 of about 34,800 (289)
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
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]
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]
We compare a large sample of galaxies between 0.5
arxiv +1 more source
Anorectal malformations at University Teaching Hospital of Butare in Rwanda: A review of 46 operative cases [PDF]
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 (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
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
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]
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
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