My child is very small, has language delays, and other developmental issues. Where can I get more information on small stature syndromes?
The MAGIC Foundation (Maturation and Growth in Children) is an informative site and a leader in this area. This site is how I discovered my daughter’s syndrome and had her diagnosed by a neurologist who specializes in rare syndromes (Dr. Asaikar in Sacramento, CA, 916.733.8149). Today, children with small stature syndromes can receive growth hormone therapy and make great strides in closing the growth gap. My daughter has grown 5 inches in one and half years since starting growth hormone therapy.