Home > internal medicine > Peroneal muscular atrophy

Peroneal muscular atrophy

Charcot Marie Tooth (CMT), also known as hereditary motor sensory neuropathy (HMSN), has obvious genetic heterogeneity. The main clinical feature is progressive muscle weakness and atrophy of the distal extremities with sensory impairment. CMT is one of the most common inherited peripheral neuropathy (the incidence rate is about 1/2500). According to the clinical and electrophysiological characteristics, CMT can be divided into two types: CMT1 type (demyelinating type), nerve conduction velocity (NCV) slowing down (median nerve conduction velocity s), CMT2 type (axonal type), normal or mild nerve conduction velocity slowing down (median nerve conduction velocity > 38m / s). Most of them are autosomal dominant inheritance, but also autosomal recessive or X-linked inheritance.

Symptoms

Lateral femoral cutaneous neuropathy

Femoral neuralgia

Hypertensive encephalopathy

Hepatolenticular degeneration

Functional dyspepsia

Graves disease

Hyperprolactinemia

Hyperosmolar non ketosis diabetic coma

Hypercholesterolemia

Hypertriglyceridemia

Hyperkalemia

Sjogren's syndrome

Cold

Hypertensive nephropathy

Myelodysplastic syndrome

Myeloproliferative disease

Myelofibrosis

bone marrow transplantation

hepatopathy

Bone infection

Common Health Issues

Health News