Charcot-Marie-Tooth disease, axonal, with vocal cord paresis, autosomal recessive

Charcot-Marie-Tooth disease, axonal, with vocal cord paresis, autosomal recessive is a rare inherited disorder that affects the peripheral nerves. Although detailed information is limited, the condition has been noted to involve nerve function and vocal cord movement. The disease is referenced in the OMIM database (OMIM:607706) and is one of several variants of Charcot-Marie-Tooth disease. Some sources also refer to this condition using synonyms such as CMT2 with vocal cord paresis, autosomal recessive, and Charcot-Marie-Tooth disease, type 4A, axonal form. The GDAP1 gene is known to be associated with this disorder, suggesting that changes in this gene may play a role in its development.

Information about symptoms is currently limited for this condition.

This condition follows an autosomal recessive pattern of inheritance. Variations in the GDAP1 gene have been identified in association with this disorder, which suggests a genetic cause. However, detailed explanations of the underlying causes are not available.

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

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

Current research and potential future directions for understanding this condition are not well detailed at this time, and information is limited.