Congenital diaphragmatic hernia (CDH) is a rare condition that occurs when a baby's diaphragm fails to develop properly during fetal development. As a result, abdominal organs such as the stomach, liver, and intestines can push up into the chest cavity, putting pressure on the lungs and interfering with their development. This can lead to breathing difficulties at birth and potentially life-threatening complications.
CDH is usually diagnosed during a routine ultrasound in the second trimester of pregnancy. Additional tests such as MRI or fetal echocardiogram may be done to evaluate the severity of the condition and assess the baby's overall health. Once diagnosed, parents are often referred to a specialized medical center with expertise in managing CDH.
It is important for parents to be aware of the signs and symptoms of CDH and seek medical attention right away if they suspect their baby may be affected. Early diagnosis and treatment can improve the chances of a positive outcome and minimize the risk of potentially life-threatening complications.
Congenital diaphragmatic hernia (CDH) is a rare condition that affects the diaphragm, which is the muscle that separates the chest from the abdomen. In CDH, the diaphragm does not fully develop, which allows abdominal organs to move into the chest cavity and compress the lungs. This can cause breathing dif...
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