Charcot-Marie-Tooth disease, dominant intermediate A

Charcot-Marie-Tooth disease, dominant intermediate A is a rare inherited condition that affects the nerves outside the brain and spinal cord. It is one of several forms of Charcot-Marie-Tooth disease, a group of disorders that mainly affects the peripheral nerves responsible for movement and sensation in the arms and legs. Although detailed descriptions are not available from the provided sources, current information indicates an association with the CMTD1A gene. The condition is noted in the OMIM database (OMIM:620378), which serves as a reference for understanding its genetic link. Because the available definition is limited, people with this condition may experience challenges related to nerve function. The role of the CMTD1A gene suggests that the disease is inherited, and as with many genetic conditions, ongoing research may help to clarify the full range of its characteristics. Future updates might provide more detailed descriptions as scientific understanding evolves.

Information about symptoms is currently limited for this condition.

Current information links Charcot-Marie-Tooth disease, dominant intermediate A to genetic changes in the CMTD1A gene. This suggests that the condition is inherited. However, additional details about how these genetic changes cause the disease or other risk factors are not provided in the available sources.

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.