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Congenital diaphragmatic hernia in newborns
Congenital diaphragmatic hernia (CDH) is a disease caused by incomplete closure of the diaphragm during the embryonic period, leading to unilateral or bilateral diaphragm defects, and some abdominal organs enter the chest cavity through the defects, resulting in abnormal anatomical relationships. Partial defects of the diaphragm during embryonic development are the basis for the onset of this disease. It is divided into thoracic hiatus hernia, esophageal hiatus hernia and congenital retrosternal hernia.
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