The treatment for Cantrell Haller Ravich syndrome depends on the symptoms and may differ from individual to individual.
- In the case of cardiac, diaphragmatic, and other associated birth defects, surgery needs to be undergone. Most of the Cantrell syndrome cases are fatal without surgeries. In extreme cases, the affected individual may die despite undergoing surgical intervention.
- Cantrell Haller Ravich syndrome does not have any specific treatment and may be different for every individual. It may depend on a lot of factors starting from the size and type of the defects. The surgeries that need to be undergone immediately after the child’s birth may include repairing the omphalocele, sternum, diaphragm, pericardium, etc.
- Most of the time, Cantrell Haller Ravich syndrome causes other conditions as well. So, while treating Cantrell Haller Ravich syndrome, the doctors may also need to undergo certain surgeries immediately after the child’s birth to deal with the same. Once the lungs and cavities are grown appropriately, again, surgeries need to be undergone in the second stage. When the child is about two to three years old, reconstruction of the entire lower sternum needs to do.
Apart from these, other treatments for Cantrell Haller Ravich syndrome may depend on the child’s condition and symptoms.
List of symptoms
Abnormal breastbone,Structural problems in the heart vessels,Presence of hernia at birth,Hole between the ventricles at the bottom of the heart, etc
List of conditions
Abnormal pericardium morphology,Abnormal sternum morphology,Abnormality of cardiovascular morphology,Congenital diaphragmatic hernia,Omphalocele,Ventricular septal defect,etc
List of Drugs