agenesis of the corpus callosum with peripheral neuropathy
Alexander disease
autonomic peripheral neuropathy
Autosomal Recessive Peripheral Neuropathy with or without Impaired Intellectual Development
axonal neuropathy +
brachial plexus neuropathy +
Canavan disease
Cerebellar Ataxia, Neuropathy, and Vestibular Areflexia Syndrome
Cerebrocortical Degeneration of Infancy
childhood spinal muscular atrophy +
Cockayne syndrome +
Congenital Muscular Dystrophy with Severe Central Nervous System Atrophy and Absence of Large Myelinated Fibers
cranial nerve disease +
diabetic neuropathy +
Dystonia Musculorum Deformans +
erythromelalgia
Familial Amyloid Polyneuropathies +
familial encephalopathy with neuroserpin inclusion bodies
familial episodic pain syndrome +
Gerstmann-Straussler-Scheinker syndrome
Gilles de la Tourette syndrome +
Hereditary Central Nervous System Demyelinating Diseases +
Hereditary Motor Neuropathy with Myopathic Features
Hereditary Optic Atrophies +
hereditary sensory neuropathy +
Huntington's disease +
Huntington's disease-like 2
Huntington's Disease-Like Syndrome
inflammatory and toxic neuropathy +
ischemic neuropathy
Kennedy's disease
Lafora disease
Leukoencephalomyelopathy
Lipodystrophy with Congenital Cataracts and Neurodegeneration
mitochondrial DNA depletion syndrome 6
mononeuropathy +
motor peripheral neuropathy +
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)
myotonia congenita +
myotonic dystrophy type 1 +
neuritis +
neuroacanthocytosis +
neurofibromatosis +
neurogenic scapuloperoneal syndrome Kaeser type
neuromuscular disease +
neuronal ceroid lipofuscinosis +
Neuropathy, with Paraprotein in Serum, Cerebrospinal Fluid and Urine
HMSN
;
HMSN Type VII
;
HSMN
;
HSMN - hereditary sensory and motor neuropathy
;
Herditary Sensory and Motor Neuropathy
;
Hereditary Motor and Sensory Neuropathies
;
Hereditary Sensory and Motor Neuropathy
;
hereditary motor and sensory neuropathy, type VII
;
neuropathic muscular atrophy