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A congenital diaphragmatic hernia (CDH) is due to the abnormal development of the diaphragm while the fetus is forming. A defect in the diaphragm of the fetus allows one or more of their abdominal ...
Medical genetics, pediatrics. Congenital diaphragmatic hernia (CDH) is a birth defect of the diaphragm. The most common type of CDH is a Bochdalek hernia; other types include Morgagni hernia, diaphragm eventration and central tendon defects of the diaphragm. Malformation of the diaphragm allows the abdominal organs to push into the chest cavity ...
Medical genetics. Cornelia de Lange syndrome (CdLS) is a genetic disorder. People with Cornelia de Lange syndrome experience a range of physical, cognitive, and medical challenges ranging from mild to severe. Cornelia de Lange syndrome has a widely varied phenotype, meaning people with the syndrome have varied features and challenges.
Bochdalek hernia is one of two forms of a congenital diaphragmatic hernia, the other form being Morgagni hernia.A Bochdalek hernia is a congenital abnormality in which an opening exists in the infant's diaphragm, allowing normally intra-abdominal organs (particularly the stomach and intestines) to enter into the thoracic cavity.
CdLS (Cornelia de Lange Syndrome) is a rare genetic disorder that affects about 1 in every 10,000 babies born in the US. This disorder can cause a range of symptoms, including physical, medical ...
Congenital diaphragmatic hernia: This condition happens when a hole in the diaphragm restricts lung development due to abdominal content entering the chest through the hole. A surgery known as ...
3 min read. Diaphragm flutter — also known as diaphragmatic flutter or diaphragmatic myoclonus — is a rare disorder in which your diaphragm experiences repeated involuntary contractions. The ...
VACTERL association. The VACTERL association (also VATER association, and less accurately VACTERL syndrome) refers to a recognized group of birth defects which tend to co-occur (see below). This pattern is a recognized association, as opposed to a syndrome, because there is no known pathogenetic cause to explain the grouped incidence.
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