Results 21 to 30 of about 30,650 (133)

Unusual occurrence of acquired hypoganglionosis following surgery for Hirschsprung's disease

Journal of Pediatric Surgery Case Reports, 2023
Purpose: Acquired hypoganglionosis or aganglionosis after surgery for Hirschsprung's disease is a littler described situation. To investigate and describe the mechanism of acquired aganglionosis or hypoganglionosis following sugery in the pulled-through ...
S. Houidi, S. Sahli, A. Zouaoui, Y. Mansouri, R. Doghri, K. Mrad, R. Jouini   +6 more
doaj   +1 more source

Experience with the redo pull-through for hirschsprung's disease

Journal of Indian Association of Pediatric Surgeons, 2019
Aim: This study aims to evaluate the need of Redo pull-through (Re PT) procedures for Hirschsprung's disease (HD) and suggest preventive strategies.
Devendra K Gupta, Kashish Khanna, Shilpa Sharma   +2 more
doaj   +1 more source

Role of SoxE transcription factors in development and disease

Developmental Dynamics, EarlyView.
Abstract Sox8, Sox9, and Sox10 arose by multiple rounds of genome duplications from a single SoxE gene in ancestral vertebrates. In this review, we will briefly discuss the molecular structure and function of SoxE transcription factors and their evolutionary origin. We will then discuss their expression, function, and developmental disorders.
Merin Lawrence, Gerhard Schlosser
wiley   +1 more source

HIRSCHSPRUNG'S DISEASE: A COMPARISON OF SWENSON'S AND SOAVE'S PULL-THROUGH METHODS

The Iraqi Journal of Medical Sciences, 2016
Background: Hirschsprung's disease or the congenital intestinal aganglionosis is the result of arrested fetal development of the myentric nervous system, but the precise pathogenic mechanisms involved are unknown.
Ahmed Z Zain, Sara Z Fadhil
doaj   +4 more sources

Diagnostic challenge of concomitant small bowel atresia and Hirschsprung's disease

Journal of Pediatric Surgery Case Reports, 2022
The incidence of ileal atresia ranges from 1/5000 to 1/12000 births. The incidence of Hirschsprung's disease is 1/5000.The combination of Hirschsprung disease and ileal atresia during infancy seems to be a rare event and the exact incidence of the ...
I. Belbahri, G. Fusi, Thibault Planchamp T, S. Mouttalib, L. Carfagna, A. Le Mandat, O. Abbo   +6 more
doaj   +1 more source

Parenteral nutrition and hospital outcomes in Australian adults: A descriptive cohort study

Journal of Parenteral and Enteral Nutrition, EarlyView.
Abstract Background There is limited information regarding real‐world use of parenteral nutrition in hospitals. The objective of the study was to provide a real‐world description of parenteral nutrition administration in hospitalized patients. Methods This was a descriptive cohort study in 507 hospitalized adults who received parenteral nutrition at ...
Frank M. P. van Haren, Sumeet Rai, Andrew Thomson, Josie Russell‐Brown, Mary Nourse, Shakira Spiller, Louise Herlihy, Sean Weng Chan, Peter Velloza, Matthew H. Anstey, Robert N. Palmer, Bianca Mammana, Tania Elderkin, Adam Visser, Matt Brain, Sarah Mineall, Emma J. Ridley   +16 more
wiley   +1 more source

Congenital short bowel syndrome: Clinical aspects by systematic review

JPGN Reports, EarlyView.
Abstract Objectives Congenital short bowel syndrome (CSBS) is a rare intestinal disorder characterized by inborn shortening of the bowel with mainly mutations in Coxsackie and Adenovirus receptor‐like membrane protein (CLMP) and Filamin A (FLNA) genes.
Barblin Remund, Susanne Schibli, Christiane Sokollik   +2 more
wiley   +1 more source

The advances of genetics research on Hirschsprung's disease

Pediatric Investigation, 2018
Hirschsprung's disease (HSCR) is a rare and complex congenital disorder characterized by the absence of the enteric neurons in lower digestive tract with an incidence of 1/5 000.
Juntao Ke, Ying Zhu, Xiaoping Miao
doaj   +1 more source

Congenital intestinal hypoganglionosis: A radiologic mimic of Hirschsprung's disease

Radiology Case Reports, 2019
Intestinal hypoganglionosis or isolated hypoganglionosis is a rare entity with a clinical and radiologic presentation that can mimic Hirschsprung's disease in the neonatal period.
Gayathri Sreedher, MD, Aaron Garrison, MD, Robert Novak, MD, FAAP, Matthew Keisling, DO, FCAP, FASCP, Shankar Srinivas Ganapathy, MD   +4 more
doaj   +1 more source

Congenital Intraoral Synechiae: A Scoping Review of Airway, Feeding, and Surgical Management

Otolaryngology–Head and Neck Surgery, EarlyView.
Abstract Objective To map the existing literature on congenital intraoral synechiae and summarize reported anatomic patterns, clinical presentation, associated anomalies/syndromes, and outcomes to inform standardized diagnostic and therapeutic approaches. Data Sources PubMed, CINAHL, Embase, Web of Science, and Google Scholar were searched from January
Jason Bernier, Mathieu Bergeron
wiley   +1 more source