Service Tree

The Service Tree lists all services in "branched" groups, starting with the very general and moving to the very specific. Click on the name of any group name to see the sub-groups available within it. Click on a service code to see its details and the providers who offer that service.

Malan Syndrome

Taxonomy Code: YF-3000.4875

A rare genetic disorder caused by a mutation in the NFIX gene that affects the rate of growth before or after birth in multiple areas, including bones, muscles, organs, and skin. It is characterized by above average height, advanced bone age, congenital heart defects, enlarged and elongated facial features, joint hypermobility, lack of muscle tone, and skeletal malformations. Symptoms can also include anxiety, intellectual disability, hearing impairments, speech delays, vision loss, and seizures.

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