Distal hereditary motor neuropathy type V — Definition

Distal kalıtsal motor nöropati tip V; distal hereditary motor neuropathic type V is a rare genetic disease, characterized by dystal muscle weakness and atrophy especially in hands and feet. The autozomal dominant inheritance shows paterni and usually starts at adult ages. The disease occurs as a result of progressive degeneration of motor neurons in the peripheral nervous system, and sensory loss is not typically seen.

The Turkish equivalent of "Distal hereditary motor neuropathy type V" is Distal kalıtsal motor nöropati tip V.

This term belongs to the Diseases category.