The Sord Deficiency Webinar  recording,  from Hereditary Neuropathy Foundation in America, would be highly relevant for patients with a positive SORD mutation genetic test. This mutation is only reported in families with recessive inheritance. The therapies in the webinar would be directed specifically for SORD mutation families.

The Webinar discusses the SORD deficiency mutation, it causes and effect, and a investigational new treatment – (AMERICA)

Please Note:

This webinar on treatment would not be for other types of CMT2 or distal motor neuropathy caused by other genes as sorbitol deficiency is not present in these forms of neuropathy.  View the webinar