Аутосомно-доминантная болезнь Шарко-Мари-Тута типа 2, вследствие мутации в гене TFG

A rare, axonal hereditary motor and sensory neuropathy characterized by adult onset of slowly progressive distal muscle weakness and atrophy, decreased deep tendon reflexes of lower limbs, and mild distal sensory loss leading to gait difficulties in most patients.