How can you get Achondroplasia?

Achondroplasia is a genetic condition that affects bone growth. It is caused by a mutation in the FGFR3 gene. This gene is responsible for producing a protein that helps to control the growth of bones. When the gene is mutated, it produces a defective protein that leads to the development of Achondroplasia.

Achondroplasia is an autosomal dominant condition, which means that only one copy of the mutated gene is needed to cause the condition. In most cases, people with Achondroplasia inherit the mutated gene from one of their parents. However, in about 10% of cases, the mutation occurs spontaneously.

There is no cure for Achondroplasia, but there are treatments that can help to improve the symptoms. These treatments may include surgery to lengthen the limbs, medication to help with pain and growth hormone therapy.