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Congenital Diaphragmatic Hernia
Congenital diaphragmatic hernia (CDH) occurs when the diaphragm does not develop completely before birth. This leaves an opening through which organs such as the intestines, stomach or liver may move into the chest.
The condition may be identified during pregnancy or after birth. Its severity varies from one child to another, so treatment is planned according to the baby's breathing, lung development and overall condition.
At Aster Hospitals, our paediatric surgery team provides assessment and treatment planning for children with congenital conditions affecting the diaphragm and chest.
Congenital diaphragmatic hernia (CDH) is a birth defect in which an opening in the diaphragm allows organs from the abdomen to move into the chest. The diaphragm is a muscle that separates the chest from the abdomen and supports normal breathing. When abdominal organs occupy space in the chest, the development of the lungs may be affected.
The main types of congenital diaphragmatic hernia include:
The child's symptoms and treatment needs depend on the location of the defect and the organs involved.
CDH develops during pregnancy when the diaphragm does not form normally. The exact reason why this happens is not always known. Genetic factors, developmental changes and other influences may be involved in some cases.
The condition is not usually caused by anything a parent did during pregnancy. A specialist may recommend additional assessments to identify associated abnormalities and understand the child's overall health.
The symptoms of congenital diaphragmatic hernia depend on the size of the defect and how much it affects lung development. Possible signs include:
A newborn with suspected CDH requires prompt assessment and specialist medical care at a leading paediatric hospital for seamless recovery.
Some cases are detected during a routine antenatal ultrasound. After birth, the condition may be suspected when a baby develops breathing difficulties or unusual examination findings. Investigations may include:
The medical team uses the findings to assess the severity of the condition and plan the next steps.
Treatment of CDH depends on the following:
Recovery varies according to lung development, the size of the defect and any associated medical problems. Some children require continued respiratory support after surgery, while others need monitoring for feeding difficulties, growth concerns or breathing problems.
At Aster Hospitals, our paediatric surgery team supports families through assessment, treatment planning and postoperative care. The care plan may include:
Book your appointment with our paediatric thoracic surgery team at Aster Hospitals to discuss your child's congenital diaphragmatic hernia and available treatment options.
Our team of experienced and board-certified paediatric surgeons evaluates children with congenital conditions affecting the diaphragm and chest. During a consultation, parents can discuss the diagnosis, treatment options, surgical approach and expected recovery.
Families looking for a congenital diaphragmatic hernia surgeon can arrange an appointment to understand their child's condition and the care that may be required.
Yes. Some cases are identified during an antenatal ultrasound. Further assessments may be recommended to evaluate lung development, the position of abdominal organs and the care required after delivery.
Surgery is generally needed to close the diaphragm defect, but the timing depends on the baby's breathing, lung development and overall stability. The medical team determines when repair can be performed safely.
Recovery varies according to the severity of the condition and the development of the lungs. Some children recover well, while others may need ongoing monitoring for breathing, feeding or growth-related concerns.
Last updated: 04-11-2026