The long-term outlook for children with AADC deficiency can vary depending on the severity of the condition, the child’s age at diagnosis, and their response to treatment. Without treatment, AADC deficiency is a progressive, life-shortening disorder that can lead to severe disability. However, with early diagnosis and treatment—particularly with gene therapy—the outlook has improved for some children. While gene therapy has shown positive results in clinical trials, the long-term benefits are still being evaluated.
Surgeries can address complications such as severe feeding difficulties or respiratory issues; these types of procedures include:
- G-tube placement: A gastrostomy tube can help with feeding when a child has difficulty swallowing or maintaining proper nutrition.
- Tracheostomy: A procedure that creates a small hole in the front of the neck to allow air to enter the lungs directly through a tube, helping improve breathing.
- Deep brain stimulation (DBS): In some cases, implanting a device that delivers electrical impulses to specific areas of the brain may help manage movement disorders associated with AADC deficiency.
At Boston Children’s, surgery is considered part of a comprehensive treatment plan that includes physical, speech, and occupational therapy services to manage symptoms and improve the overall quality of life for children with AADC deficiency.