"Camptomelic syndrome is a rare genetic disorder that affects the development of certain bones in the body. It is most commonly found in children, but it can also affect adults. Camptomelic syndrome is diagnosed through a physical exam, and it can be confirmed with X-rays and/or CT scans.
Camptomelic syndrome is caused by a mutation in the FGFR2 gene. This gene controls how your body grows bones, especially those of the hands and feet. When a pe Read More
Le jeune syndrome is a rare genetic disorder that affects the development of bones and joints, as well as the function of the heart and lungs. It is caused by a mutation in the JAG1 gene, which can affect any organ system in the body. There are several risk factors that can increase your chances of developing Jeune syndrome. 1. Family history: The first is having a family history of the condition. If Read More