DiGeorge syndrome is a genetic disorder that's usually noticeable at birth. Children with the condition can have heart defects, learning difficulties, a cleft palate and potentially many other problems. In almost all cases, these symptoms and features result from a missing piece of chromosome – a genetic fault, or mutation, called 22q11 deletion.

?
Ask Question
AboutMyClinic
SmartSite created on AboutMyClinic.com
Disclaimer: The information provided here should not be used during any medical emergency or for the diagnosis or treatment of any medical condition. The information is provided solely for educational purpose and should not be considered a substitute for medical advice.