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Nervous System Diseases > Nervous System Malformations > Hereditary Sensory and Autonomic Neuropathies
Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Congenital Abnormalities > Nervous System Malformations > Hereditary Sensory and Autonomic Neuropathies
Nervous System Diseases > Neuromuscular Diseases > Peripheral Nervous System Diseases > Polyneuropathies > Hereditary Sensory and Autonomic Neuropathies
Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Genetic Diseases, Inborn > Heredodegenerative Disorders, Nervous System > Hereditary Sensory and Autonomic Neuropathies
Nervous System Diseases > Neurodegenerative Diseases > Heredodegenerative Disorders, Nervous System > Hereditary Sensory and Autonomic Neuropathies

Terme préférentiel

Hereditary Sensory and Autonomic Neuropathies  

Type

  • mesh:Descriptor

Définition

  • 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)

Concept générique

Concepts spécifiques

Concepts associés

Synonyme(s)

  • HSAN
  • HSAN (Hereditary Sensory Autonomic Neuropathy)
  • Neuropathies, Hereditary Sensory and Autonomic
  • Sensory and Autonomic Neuropathies, Hereditary

Qualificatif(s) autorisé(s)

Traductions

URI

http://data.loterre.fr/ark:/67375/JVR-VN6PDF3J-5

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RDF/XML TURTLE JSON-LD Date de création 08/11/1999, dernière modification le 30/06/2018