Thursday, June 18, 2009

Treatment for DiGeorge syndrome (Velocardiofacial Syndrome)

Velocardiofacial Syndrome

Specific treatment for DiGeorge syndrome will be determined by your child's physician based on the following:

- your child's age, overall health, and medical history
- the extent of the disease
- the type of disease
- your child's tolerance for specific medications, procedures, or therapies
expectations for the course of the disease
- your opinion or preference

Treatment will also depend on the particular features in any given child and may include the following:

- Heart defects will be evaluated by a cardiologist.
- A plastic surgeon and a speech pathologist will evaluate cleft lip and/or palate.
- Speech and gastrointestinal specialists will evaluate feeding difficulties.
- Immunology evaluations should be performed in all children with this deletion. To monitor T-cell disorder and recurrent infections, live viral vaccines should be avoided and all blood products for transfusions (if needed) should be irradiated unless cleared by an immunology physician.

In severe cases where immune system function is absent, bone marrow transplantation is required.

Many newborns with this deletion will benefit from early intervention to help with muscle strength, mental stimulation, and speech problems. Basically, treatment is dependent upon the specific symptoms seen in any given child.

Velocardiofacial Syndrome

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