Charcot-Marie-Tooth disease recessive intermediate D

Charcot-Marie-Tooth disease recessive intermediate D is a rare inherited condition that affects the nerves. It is caused by a mutation in the COX6A1 gene, which plays an important role in the production of energy in cells. Changes in this gene can lead to problems with nerve function, and this condition is one of several forms of Charcot-Marie-Tooth disease. People with this condition may experience various signs and symptoms due to nerve damage. Although specific details about the range of symptoms are not fully described here, the underlying cause is clearly linked to the genetic mutation in COX6A1. More research is needed to better understand all aspects of this condition and its effects on nerve function.

Information about symptoms is currently limited for this condition.

The condition is caused by a mutation in the COX6A1 gene. Because the disorder is inherited in an autosomal recessive pattern, two copies of the mutated gene are required for the condition to occur. More detailed information about risk factors and genetic variations is currently limited.

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.