Meckel syndrome, type 6

Meckel syndrome, type 6 is a rare inherited condition that is caused by a mutation in the CC2D2A gene. This condition is part of the group of disorders known as Meckel syndrome, which typically affects many parts of the body due to its genetic origins. The description of the disease highlights that the underlying cause of this syndrome is linked to changes in this specific gene. People with this condition may have complex health challenges, although detailed information about the range of features and body systems affected is limited. Studies and reports focus on the genetic basis of the disorder and its classification within rare syndromes, which is confirmed through the mutation in CC2D2A. This overview is based on available definition information and recognized database entries for this rare disorder.

Information about symptoms is currently limited for this condition.

The cause of Meckel syndrome, type 6 is a mutation in the CC2D2A gene. This abnormal change in the gene leads to the development of the syndrome. Genetic changes like this one are the key factor behind the condition.

Information about treatment is currently limited for this condition.

Information about prognosis is currently limited for this condition.

Information about research is currently limited for this condition.