Results 71 to 80 of about 303,873 (178)

Fryns syndrome in children with congenital diaphragmatic hernia

, 2002
Fryns syndrome is characterized by multiple congenital anomalies including Congenital Diaphragmatic Hernia (CDH), and has a reported poor prognosis with a survival rate during the neonatal period of approximately 15%.
Jaksic, Tom, Congenital Diaphragmatic Hernia Study Group, Langham, Jr, Max R, Lally, Kevin P, Wilson, Jay M, Lally, Pamela A, Hirschl, Ronald B, Hardin, Jr, William D, Neville, Holly L   +8 more
core   +1 more source

Multipotent mesenchymal stromal cell therapy for a neonate with congenital diaphragmatic hernia and adhesive small bowel obstruction

The Turkish Journal of Pediatrics
Background. In the last decade, therapy using multipotent mesenchymal stromal cells (MSCs) has offered hope for regenerating the lungs of preterm babies with chronic lung disease. Due to similar disease mechanisms, it is logical to explore the potential
Şükran Yıldırım, Aliye Kandırıcı
doaj   +1 more source

Newborn male presented with congenital diaphragmatic hernia and choledochal cyst: A case report

Journal of Pediatric Surgery Case Reports, 2015
Infants with congenital diaphragmatic hernia (CDH) have an increased incidence of associated malformations, ranging from 10% to 50% higher than the general population [1–5]. Choedochal cysts, congenital cystic dilations of the biliary tree, are anomalies
Daniel Krebs, Richard S. Herman, Christopher Blewett   +2 more
doaj   +1 more source

Co‐Occurring Non‐Cardiac Congenital Anomalies Among Cases With Congenital Heart Defects

American Journal of Medical Genetics Part A, Volume 200, Issue 9, Page 1953-1972, September 2026.
ABSTRACT Cases with congenital heart defects (CHD) often have other associated anomalies. The aim of this investigation was to assess the prevalence and the types of co‐occurring anomalies in CHD in a well‐defined population. The anomalies co‐occurring with CHD were ascertained in all live births, stillbirths and terminations of pregnancy for fetal ...
Claude Stoll, Yves Alembik, Marie‐Paule Roth   +2 more
wiley   +1 more source

Identification of major congenital malformations based on healthcare databases in France: A proof‐of‐concept study using the epi‐meres nationwide mother–child register

British Journal of Clinical Pharmacology, Volume 92, Issue 9, Page 3037-3048, September 2026.
Abstract Aim Besides registries, healthcare databases can provide useful information for assessing the frequency of major congenital malformations (MCMs) and investigating their risk factors, particularly medication exposures. This study aimed to assess the validity of MCMs identification based on French national, comprehensive healthcare databases ...
Tom Duchemin, Lise Marty, Jérôme Drouin, Sara Miranda, Jérémie Botton, Valérie Olié, Alain Weill, Rosemary Dray‐Spira   +7 more
wiley   +1 more source

CLINICAL CASE OF CONGENITAL DIAPHRAGMATIC HERNIA [PDF]

, 2023
Despite current advances in obstetrics and pediatric surgery, the survival rate of newborns with congenital diaphragmatic hernia does not exceed 50 %. This article describes a clinical case of a child with congenital diaphragmatic hernia with a favorable
Елена Павловна Царюк, Дмитрий Александрович Маисеенко, Наталья Юрьевна Колмакова, Олеся Владимировна Кляшторная, Надежда Владимировна Головкина, Аида Анушавановна Исаханян   +5 more
core  

Congenital diaphragmatic hernia in neonate: A retrospective study about 28 observations

African Journal of Paediatric Surgery, 2012
Objective: Our purpose was to review our experience with congenital diaphragmatic hernia emphasizing diagnosis, management, and outcome. Study Design: We conducted a retrospective review of all cases of babies with congenital diaphragmatic hernia ...
Rachid Khemakhem, Basma Haggui, Houda Rahay, Faouzi Nouira, Awatef Charieg, Sofiane Ghorbel, Mahdi Trifa, Said Jlidi, Sonia Ben Khalifa, Beji Chaouachi   +9 more
doaj   +1 more source

Thoracoscopic repair of neonatal congenital diaphragmatic hernia

, 2016
Purpose: To describe the surgical technique and criteria for neonatal congenital diaphragmatic hernia (CDH) repair. Methods: CDH repairs were carried out by a thoracoscopic approach between February 2013 and April 2014.
Nagayasu, Takeshi, Obatake, Masayuki, Yamane, Yusuke, Taura, Yasuaki, Yoshida, Takuya   +4 more
core  

In utero incarceration of congenital diaphragmatic hernia

, 2011
In utero diagnosis of incarcerated congenital diaphragmatic hernia has never been reported. In our case, congenital diaphragmatic hernia presented at 34 weeks of gestation with dilated bowel loops, pleural effusion, and ascites on fetal ultrasound ...
Török, Olga, Cserni, Tamás, Nagy, Andrea Judit, Olga Torok, Peter Cserni, Tamas Cserni, Andrea Nagy, Balla, György, Gyorgy Balla, Laszlo Orosz, Istvan Pataki, Anna May Long, Long, Anna May, Cserni, Péter, Edit Polonkai, Polonkai, Edit, Orosz, László, Pataki, István   +17 more
core   +1 more source

AGRN‐, LRP4‐, MUSK‐Related CMS: Clinical, Neurophysiological, Morphological, Genetic and Pathological Mechanisms

Muscle &Nerve, Volume 74, Issue S1, Page S31-S40, September 2026.
ABSTRACT Congenital myasthenic syndromes (CMS) are inherited disorders caused by mutations in genes encoding proteins essential for neuromuscular junction (NMJ) function. Pathogenic variants have been identified in more than 35 genes, underscoring the complexity of synaptic biology and the wide range of mechanisms that can compromise neuromuscular ...
Rocio‐Nur Villar‐Quiles, Damien Sternberg, Marie‐Christine Nougues, Arnaud Isapof, Bruno Eymard, Stéphanie Bauché   +5 more
wiley   +1 more source