Results 91 to 100 of about 8,937 (249)
Colon pouch syndrome. In the spectrum of the anorectal malformaciotions
Congenital colon pouch syndrome, is an infrequent clinical condition in which the colon is totally o partially replaced by a cystic dilatation, and is associated with an anorectal malformation; which may be a urinary tract fistula, a vaginal or vestibule
Santos Jasso Karla Alejandra+1 more
doaj +1 more source
Asuhan Keperawatan Pada An. I dengan Gangguan Sistem Pencernaan: Malformasi Anorektal Post Posterio Sagital Ano Recto Plasty (PSARP) di Ruang Melati 2 Rumah Sakit Umum Daerah Dr.Moewardi Surakarta [PDF]
Background: Incidents of anorectal malformation are ranged from 1500-5000 live births with slightly more for male. About 20% - 75% of infants with anorectic malformation are also suffering other anomaly.
, Siti Arifah, S.Kp., M.Kes+1 more
core
ABSTRACT Objective To analyze comprehensively the incidence, antenatal ultrasound characteristics and prognostic implications of antenatal pop‐off mechanisms of the fetal urinary system in pregnancies with suspected fetal megacystis. Methods This was a retrospective multicenter study of pregnancies with suspected fetal megacystis conducted across all ...
L. A. M. Brinkman+9 more
wiley +1 more source
Birth prevalence of anorectal malformations in England and 5-year survival: a national birth cohort study [PDF]
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.
Curry, Joe I+4 more
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Association of Anaesthetists guidelines: the use of blood components and their alternatives
Summary Background The administration of blood components and their alternatives can be lifesaving. Anaemia, bleeding and transfusion are all associated with poor peri‐operative outcomes. Considerable changes in the approaches to optimal use of blood components and their alternatives, driven by the findings of large randomised controlled trials and ...
Akshay Shah+12 more
wiley +1 more source
Anterior sacral meningocele (ASM) and neural tube defect are well-known clinical entity. Hirschsprung's disease is rarely associated with ASM, but the association with anorectal malformation is common.
Md Hadiuzzaman+3 more
doaj +1 more source
Normal Anal Sensibility in Patients Born With Anorectal Malformations
Normal anal sensibility can be present in ARM patients diagnosed with all types of ARM after they have been treated with corrective surgery. Anal sensibility was better in those with a functional IAS. This means that the IAS, present in the distal end of the fistula, should be spared as much as possible to preserve anal sensibility. In this way, aiming
Venla E. C. den Hollander+2 more
wiley +1 more source
Rare association of prune belly syndrome with pouch colon
M Ragavan1, U Haripriya1, PV Pradeep1, J Sarvavinothini21Department of Endocrine Surgery, 2Department of Anaesthesia, Narayana Medical College and Superspeciality Hospital, Nellore, Andhra Pradesh, IndiaAbstract: Prune belly syndrome is a triad ...
M Ragavan+3 more
doaj
Introduction: Anorectal malformation (ARM) associated esophageal atresia (EA) with tracheoesophageal fistula (TEF) spawns special therapeutic propositions. The outcome of these patients banks on numerous factors.
Ajay Narayan Gangopadhyay+1 more
doaj +1 more source
Sacral agenesis: a pilot whole exome sequencing and copy number study [PDF]
Background: Caudal regression syndrome (CRS) or sacral agenesis is a rare congenital disorder characterized by a constellation of congenital caudal anomalies affecting the caudal spine and spinal cord, the hindgut, the urogenital system, and the lower ...
Campbell, Desmond D.+11 more
core +1 more source