Charcot-Marie-Tooth disease, axonal, type 2FF

Charcot-Marie-Tooth disease, axonal, type 2FF—also known as CMT2FF or Charcot-Marie-Tooth neuropathy—is a rare inherited condition that affects the peripheral nerves. Although detailed information is limited, the condition has been linked to a change in the CADM3 gene, and its association is noted in the OMIM database (OMIM:619519). Because the overall characteristics of this condition are not fully understood, additional research is needed. Many details about its onset, progression, and impact on nerve function remain under investigation.

Information about symptoms is currently limited for this condition.

Research has associated this condition with changes in the CADM3 gene. The genetic link is supported by records in the OMIM database (OMIM:619519). However, details about the precise genetic mechanism and inheritance pattern are limited at this time.

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.