Peripheral motor neuropathy-dysautonomia syndrome

Peripheral motor neuropathy-dysautonomia syndrome is characterized by distal, slowly progressive muscular weakness, childhood-onset amyotrophy, autonomic dysfunction characterized by profuse sweating, distal cyanosis related to cold weather, orthostatic hypotension, and esophageal achalasia. It has been described in two sisters. Inheritance appears to be autosomal recessive.

Also known as: Lisker-Garcia-Ramos syndrome, motor neuropathy, peripheral, with dysautonomia

0 clinical trials for this condition and its sub-types, 0 tagged with Peripheral motor neuropathy-dysautonomia syndrome itself.