Hereditary Sensory and Motor Neuropathy

Synonyms

CMT4f

Charcot Marie Tooth Disease, Type 3

Charcot-Marie-Tooth Disease, Demyelinating, Type 4f

Charcot-Marie-Tooth Disease, Type 3

Dejerine Sottas Disease

Dejerine Sottas Neuropathy

Dejerine Sottas Syndrome

Dejerine-Sottas Disease

Dejerine-Sottas Hypertrophic Neuropathy

Dejerine-Sottas Neuropathy

Dejerine-Sottas Syndrome

Disease, Dejerine-Sottas

HMSN

HMSN Type III

HMSN Type IIIs

HMSN Type VII

HMSN Type VIIs

HMSN3

Herditary Sensory and Motor Neuropathy

Hereditary Motor and Sensory Neuropathies

Hereditary Motor and Sensory Neuropathy

Hereditary Motor and Sensory Neuropathy 3

Hereditary Motor and Sensory Neuropathy Type III

Hereditary, Type III, Motor and Sensory Neuropathy

Hereditary, Type VII, Motor and Sensory Neuropathy

Hypertrophic Neuropathy of Dejerine Sottas

Hypertrophic Neuropathy of Dejerine-Sottas

Neuropathies, Hereditary Motor and Sensory

Neuropathy, Dejerine-Sottas

Syndrome, Dejerine-Sottas

Type VII, HMSN

A group of slowly progressive inherited disorders affecting motor and sensory peripheral nerves. Subtypes include HMSNs I-VII. HMSN I and II both refer to CHARCOT-MARIE-TOOTH DISEASE. HMSN III refers to hypertrophic neuropathy of infancy. HMSN IV refers to REFSUM DISEASE. HMSN V refers to a condition marked by a hereditary motor and sensory neuropathy associated with spastic paraplegia (see SPASTIC PARAPLEGIA, HEREDITARY). HMSN VI refers to HMSN associated with an inherited optic atrophy (OPTIC ATROPHIES, HEREDITARY), and HMSN VII refers to HMSN associated with retinitis pigmentosa. (From Adams et al., Principles of Neurology, 6th ed, p1343)