Results 41 to 50 of about 6,430 (192)

Five-year experience of anorectal malformation with oesophageal atresia in tertiary care hospital

African Journal of Paediatric Surgery, 2020
Aim: We had done this study for TEF with Anorectal malformation and TEF with no Anorectal malformation in terms of age, sex, surgical outcomes and mortality.
Sarita Chowdhary, Pranay Panigrahi, Rakesh Kumar   +2 more
doaj   +1 more source

15-Year-old with neglected recto-vestibular fistula in western Uganda: a case report

Journal of Medical Case Reports, 2021
Background Teenage and late presentation of anorectal malformations are not uncommon in developing world. Some of the reasons for late presentation include but not limited to illiteracy, poverty, lack of awareness, and limited trained pediatric surgeons.
Felix Oyania, Meera Kotagal, Martin Situma   +2 more
doaj   +1 more source

Intestinal Atresia in Finland: Maternal Risk Factors, Prevalence, Associated Anomalies and Survival

Acta Paediatrica, EarlyView.
ABSTRACT Aim We aimed to investigate prevalence, associated anomalies and survival of congenital intestinal atresia and to examine maternal risk factors for jejunoileal atresia (JIA). Methods All children born with, or pregnancies terminated because of, JIA or colonic atresia (CA) in Finland during 1987–2019 were identified from the Finnish Register of
Esko Tahkola, Arimatias Raitio, Ilkka Helenius, Johanna Syvänen, Teemu Kemppainen, Eliisa Löyttyniemi, Maarit K. Leinonen, Mika Gissler, Topi Luoto, Mikko P. Pakarinen   +9 more
wiley   +1 more source

Esophageal lung with rare associated vascular and anorectal malformations

Radiology Case Reports, 2018
Esophageal lung is a rare communicating bronchopulmonary foregut malformation in which the main bronchus arising from the trachea is absent. The affected lung is usually hypoplastic and aerated via an anomalous airway originating from the esophagus ...
Ali Alsaadi, SB-Rad, Hamdi A. Alsufiani, MD, Mohammad D. Allugmani, MD, Altaf Hussain Gora, MD   +3 more
doaj   +1 more source

Mortality Patterns and Phenotypic Clusters in Trisomy 13: A Population‐Based Study From Japan

American Journal of Medical Genetics Part A, Volume 200, Issue 2, Page 329-338, February 2026.
ABSTRACT Trisomy 13, the third most common autosomal trisomy after trisomy 21 and trisomy 18, is associated with a significantly high infant mortality rate. However, large‐scale studies examining causes of death in trisomy 13 remain scarce. Therefore, we aimed to better understand the mortality patterns.
Narumi Kato, Naho Morisaki, Akinori Moriichi   +2 more
wiley   +1 more source

Regenerative Approach With Autologous Fat Grafting and Stem Cells for the Treatment of Post‐Traumatic Anal Incontinence: A Case Report

Clinical Case Reports, Volume 14, Issue 1, January 2026.
ABSTRACT Autologous fat grafting enriched with mesenchymal stem cells is a promising minimally invasive regenerative therapy for post‐traumatic anal incontinence. This approach may restore continence and quality of life, even when structural sphincter defects persist.
Alexandre da Silva Nishimura, Giuliana Donoso Andrade Silva, Vitor Holmo Figueira, Eduardo Isaac Nishimoto, Pedro Luiz Nishimura Menardi, Igor Rincon Gonçalves Passaglia, Sabrina Thalita dos Reis   +6 more
wiley   +1 more source

Acute kidney injury due to obstructive nephropathy caused by fecal impaction in a renal transplant patient - A case report

Indian Journal of Transplantation, 2021
Acute kidney injury (AKI) remains a major complication after transplantation; its common causes include acute rejection and urinary tract obstruction. Here, we report an unusual case of a 16-year-old renal transplant patient with congenital anomalies of ...
Tomoo Kise, Shigeru Fukuyama, Masatsugu Uehara   +2 more
doaj   +1 more source

Retrospective case‐control study of nutritional and respiratory status in children with type III esophageal atresia

Journal of Pediatric Gastroenterology and Nutrition, Volume 82, Issue 1, Page 184-193, January 2026.
Abstract Objectives To evaluate the impact of undernutrition in school‐aged children born with type III esophageal atresia (EA), and to determine its potential risk factors, including their respiratory history and status assessed by pulmonary function tests at school‐age. Methods Retrospective multicentre cohort study encompassing patients born between
Marie‐Alix Chansou, Rony Sfeir, Arnaud Bonnard, Véronique Rousseau, Thomas Gelas, Audrey Guinot, Edouard Habonimana, Pascale Micheau, Aline Ranke, Isabelle Talon, Sabine Irtan, Thierry Lamireau, Pierre‐Yves Rabattu, Frédéric Elbaz, Nicolas Kalfa, Nicoleta Panait, Virginie Fouquet, Hubert Lardy, Aurélien Scalabre, Philippe Buisson, Marc Margaryan, Frédéric Auber, Céline Grosos, Corinne Borderon, Cécilia Tölg, Jeanne Goulin, Guillaume Podevin, Frédéric Gottrand, Françoise Schmitt   +28 more
wiley   +1 more source

Defining the molecular pathologies in cloaca malformation: similarities between mouse and human

Disease Models & Mechanisms, 2014
Anorectal malformations are congenital anomalies that form a spectrum of disorders, from the most benign type with excellent functional prognosis, to very complex, such as cloaca malformation in females in which the rectum, vagina and urethra fail to ...
Laura A. Runck, Anna Method, Andrea Bischoff, Marc Levitt, Alberto Peña, Margaret H. Collins, Anita Gupta, Shiva Shanmukhappa, James M. Wells, Géraldine Guasch   +9 more
doaj   +1 more source

Challenges following Prenatal Diagnosis of Bilateral Renal Agenesis and Spontaneous Therapy of Fetal Renal Replacement, or Transplant by Auto-Amnioinfusion in a Monoamniotic Twin Discordant Twin with Associated Postnatal Diagnosis of Anorectal Malformation [PDF]

, 2022
DJ Govani, ND Govani, DR Govani, NG Panchasara, RR Patel, PK Midha, RV Patel   +6 more
openalex   +1 more source