نتایج جستجو برای: congenital diaphragmatic hernia cdh
تعداد نتایج: 144430 فیلتر نتایج به سال:
Recurrent microdeletions of 8p23.1 that include GATA4 and SOX7 confer a high risk of both congenital diaphragmatic hernia (CDH) and cardiac defects. Although GATA4-deficient mice have both CDH and cardiac defects, no humans with cardiac defects attributed to GATA4 mutations have been reported to have CDH. We were also unable to identify deleterious GATA4 sequence changes in a CDH cohort. This s...
Aim: Chylothorax is a recognized complication after surgery for congenital diaphragmatic hernia (CDH) in a neonate. Management strategies for chylothorax include cessation of enteral feedings, repeated aspiration, chest drainage, and total parenteral nutrition. It is important to determine which is the better plan for treatment of chylothorax after repair of CDH. The authors report successful m...
introduction: combination of congenital diaphragmatic hernia (cdh) and anorectal malformation (arm) is rare. in this report, we describe a combination of imperforate anus and cdh in one of twins who conceived by assisted reproductive technology (art). case report: a female preterm newborn at 27 weeks of gestation was referred to our neonatal intensive care unit due to respiratory distress. she ...
BACKGROUND Eosinophilic esophagitis (EoE) is an increasingly diagnosed disease, especially in the western world. Although its pathogenesis remains poorly understood, there is strong evidence that the eosinophilic inflammation in EoE is primarily triggered by immune dysregulation secondary to allergic sensitization to dietary or aero-allergens. Recent studies have reported a higher prevalence of...
PURPOSE To evaluate the perinatal results for fetuses and neonates with left-sided congenital diaphragmatic hernia (CDH) and the role of the prenatal diagnosis in the pregnancy outcome. MATERIALS AND METHODS We reviewed data from fetuses and neonates with left-sided CDH, managed from January 2009 and December 2013 in the University Clinic Hospital, Craiova, Romania. The following data were an...
Congenital diaphragmatic hernia (CDH) is a developmental malformation characterized by defect in the diaphragm that allows abdominal viscera to move into chest cavity. A routine ultrasound screening performed during pregnancy detects over half of all cases. This paper describes two women who were prenatally diagnosed have fetus with isolated posterolateral CDH. Both mothers underwent medical ab...
BACKGROUND Congenital diaphragmatic hernia (CDH) is a life threatening birth defect. Most of the genetic factors that contribute to the development of CDH remain unidentified. OBJECTIVE To identify genomic alterations that contribute to the development of diaphragmatic defects. METHODS A cohort of 45 unrelated patients with CDH or diaphragmatic eventrations was screened for genomic alterati...
Gastric volvulus is a rare cause of recurrent abdominal pain in children. Usually it is associated with diaphragmatic pathology. A 9-year-old boy presented with recurrent abdominal pain and vomiting. Investigations confirmed a volved stomach in the left chest and a left congenital diaphragmatic hernia (CDH). Laparoscopic reduction and repair of CDH was performed successfully. The stomach was de...
Congenital diaphragmatic hernia (CDH) has an incidence of approximately 1:4000 live births. Most frequently the diaphragmatic defect is a left and posterolateral (Bochdalek) one. Prenatal diagnosis is made at ultrasonography; the relevant sonographic features will be described in the paper. Cystic adenomatoid malformation of the lung (CAML), pulmonary sequestration, bronchogenic cysts, pulmonar...
Congenital diaphragmatic hernia (CDH) is a developmental anomaly characterized by the malformation of the diaphragm and impaired lung development. In the present study, we tested several hypotheses regarding the pathogenesis of CDH, including those suggesting that the primary defect is due to abnormal 1) lung development, 2) phrenic nerve formation, 3) developmental processes underlying diaphra...
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