Joubert syndrome 14

Joubert syndrome 14 is a rare genetic condition that is part of the Joubert syndrome family. It is specifically caused by a mutation in the TMEM237 gene. This condition is recognized as one of several types of Joubert syndrome and is identified by its genetic cause. People with Joubert syndrome 14 may share features common to other Joubert syndromes. However, detailed information about the specific range of symptoms and other characteristics for this subtype is limited.

Information about symptoms is currently limited for this condition.

Joubert syndrome 14 is caused by a mutation in the TMEM237 gene. This means that changes in this gene contribute to the development of the condition. Like many genetic conditions, a mutation in a specific gene can affect various parts of the body, although detailed risk factors specific to this subtype are not extensively described.

Information about treatment options and management approaches is currently limited for this condition.

Information about the outlook and quality of life for people with this condition is currently limited.

Information about current research and future directions for Joubert syndrome 14 is currently limited.