Meckel syndrome, type 11

Meckel syndrome, type 11 is a rare genetic disorder caused by a mutation in the TMEM231 gene. This condition is one type within a group of disorders known as Meckel syndrome, where mutations in specific genes lead to abnormal development. The genetic change in TMEM231 affects the function of the protein it encodes, which is important for normal development in various tissues. Because Meckel syndrome, type 11 is classified based on its underlying genetic cause, understanding the mutation helps researchers and clinicians better understand how the disorder develops. Reliable genetic testing and examining family history can be essential in identifying and studying this condition. The information provided here is based on trusted sources such as definitions and established genetic data.

Information about symptoms is currently limited for this condition.

This condition is caused by a mutation in the TMEM231 gene. A change in this gene can lead to problems in the normal function of the protein it produces, which may affect the development of different parts of the body. The genetic nature of Meckel syndrome, type 11 means that it is inherited, and understanding the gene involved helps in grasping the cause of the disorder.

Information about treatment is currently limited for this condition.

Information about prognosis is currently limited for this condition.

Information about current research and future directions is currently limited for this condition.