Meckel syndrome 13

Meckel syndrome 13, also known as Meckel syndrome type 13 or MKS13, is a rare condition. Information about its overall characteristics is limited, but it is recognized as a genetic disorder that involves changes in a specific gene. The condition has been identified in scientific resources primarily through genetic studies and cataloged entries such as in OMIM and GARD. While detailed descriptions of its clinical features are sparse, research has indicated that a mutation in the TMEM107 gene is associated with this disorder. Because of its rarity, the full range of symptoms and the extent of the impact on different body systems are not fully described in the currently available literature.

Information about symptoms is currently limited for this condition.

The cause of Meckel syndrome 13 is linked to genetic changes. Specifically, mutations in the TMEM107 gene have been identified in people with this condition. This genetic alteration is believed to play a role in its development, although detailed information about other possible risk factors is currently limited.

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

Information about the outlook and quality of life for people with Meckel syndrome 13 is currently limited for this condition.

There is ongoing research to better understand Meckel syndrome 13, especially in relation to its genetic causes and how mutations in the TMEM107 gene affect the body. However, detailed findings and future directions are still emerging, and current research information is limited.