Congenital diaphragmatic hernia (CDH) is a developmental defect of the diaphragm that allows abdominal viscera to herniate into the chest. Affected neonates usually present in the first few minutes to hours after birth with respiratory distress that can range from mild to life-threatening.

Congenital diaphragmatic hernia (CDH) can occur on the left or the right side of the diaphragm. Learn about the difference between right and left-sided CDH.

The lung-to-head circumference ratio (LHR) is a sonographic measure proposed to identify fetuses with congenital diaphragmatic hernia (CDH) that have a poor prognosis (4).

Congenital diaphragmatic hernia (CDH) is a condition present before birth characterized by abnormal development of the diaphragm. The diaphragm normally separates the organs in the abdomen from those in the chest. The severity of CDH may range from a thinned area in part of the diaphragm, to its complete absence.

Lt CDH, liver up, using high-resolution gray-scale to demonstrate liver position UNITED STATES

Congenital diaphragmatic hernia (CDH) is a serious condition where the diaphragm—the muscle that separates the chest from the abdomen—doesn’t form properly as the fetus develops. This leaves an opening that can allow the abdominal organs to shift up into the chest, crowding the lungs and heart.

What is congenital diaphragmatic hernia? A congenital diaphragmatic hernia (CDH) occurs when a baby's diaphragm doesn't form completely during fetal development. This leaves an opening between the chest and abdominal cavities, allowing abdominal organs to herniate (protrude or enter) into the chest cavity and prevent lung development.

Congenital diaphragmatic hernia (CDH) is a relatively common major life-threatening birth defect that results in significant mortality and morbidity depending primarily on lung hypoplasia, persistent pulmonary hypertension, and cardiac dysfunction. ...

Congenital diaphragmatic hernia (CDH) is a developmental defect that requires intensive cardiorespiratory support in the perioperative period. The exemplar anomaly in CDH is pulmonary hypoplasia, which manifests as postnatal pulmonary hypertension of variable severity; however, infants with CDH also experience additional multisystem morbidity.

Congenital diaphragmatic hernia (CDH) refers to a hole in the diaphragm, the muscle that separates the organs in the chest from those in the abdomen. It is treated at the Ontario Fetal Centre in Toronto, Ontario.