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| Hereditary Sensory and Autonomic Neuropathies | Legal notice |
Other terms
Sensory and Autonomic Neuropathies, Hereditary,Neuropathies, Hereditary Sensory and Autonomic,HSAN,HSAN (Hereditary Sensory Autonomic Neuropathy),HSANs (Hereditary Sensory Autonomic Neuropathy),HSAN Type IV,Type IV, HSAN,Congenital Insensitivity to Pain with Anhidrosis,Familial Dysautonomia, Type 2,Pain Insensitivity with Anhidrosis, Congenital,HSAN 4,Insensitivity to Pain with Anhidrosis, Congenital,Insensitivity to Pain, Congenital, with Anhidrosis,Neuropathy, Congenital Sensory, with Anhidrosis,Hereditary Sensory and Autonomic Neuropathy 4,Hereditary Sensory Autonomic Neuropathy, Type 4,HSAN Type V,Type V, HSAN,Hereditary Sensory Autonomic Neuropathy, Type 5,Sensory Neuropathy, Hereditary,Hereditary Sensory Neuropathies,Hereditary Sensory Neuropathy,Neuropathies, Hereditary Sensory,Neuropathy, Hereditary Sensory,Sensory Neuropathies, Hereditary,Neuropathy, Congenital Sensory,Congenital Sensory Neuropathies,Congenital Sensory Neuropathy,Neuropathies, Congenital Sensory,Sensory Neuropathies, Congenital,Sensory Neuropathy, Congenital,Neurogenic Acroosteolysis,Acroosteolyses, Neurogenic,Acroosteolysis, Neurogenic,Neurogenic Acroosteolyses,HSN Type II,Hereditary Sensory and Autonomic Neuropathy Type 2,Hereditary Sensory Radicular Neuropathy, Recessive Form,HSAN Type II,Giaccai Type Acroosteolysis,Acroosteolysis, Giaccai Type,Type Acroosteolysis, Giaccai,Hereditary Sensory Autonomic Neuropathy, Type 2,Hereditary Sensory Radicular Neuropathy,HSN Type I,Type I, HSN,Neuropathy Hereditary Sensory Radicular, Autosomal Dominant,HSAN Type I,Type I, HSAN,Hereditary Sensory Neuropathy Type 1,HSAN 1,Neuropathy Hereditary Sensory and Autonomic Type 1,Hereditary Sensory Autonomic Neuropathy, Type 1
Description
Hereditary Sensory and Autonomic Neuropathies: A group of inherited disorders characterized by degeneration of dorsal root and autonomic ganglion cells, and clinically by loss of sensation and autonomic dysfunction. There are five subtypes. Type I features autosomal dominant inheritance and distal sensory involvement. Type II is characterized by autosomal inheritance and distal and proximal sensory loss. Type III is DYSAUTONOMIA, FAMILIAL. Type IV features insensitivity to pain, heat intolerance, and mental deficiency. Type V is characterized by a selective loss of pain with intact light touch and vibratory sensation. (From Joynt, Clinical Neurology, 1995, Ch51, pp142-4)
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- Polyradiculoneuropathy
- Polyradiculoneuropathy
- Heredodegenerative Disorders, Nervous System
- Polyneuropathies
- Polyradiculoneuropathy
- Nervous System Malformations
- Heredodegenerative Disorders, Nervous System
- Polyradiculoneuropathy
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