HSAN HSAN, typ I HSAN, typ II HSAN, typ IV HSAN, typ V HSN, typ I HSN, typ II necitlivosť na bolesť s anhidrózou, vrodená necitlivosť na bolesť s anhidrózou, kongenitálna neuropatie senzorické, dedičné
English X references
HSAN HSAN Type I HSAN Type II HSAN Type IV HSAN Type V HSN Type I HSN Type II Insensitivity to Pain with Anhidrosis, Congenital Neuropathies, Hereditary Sensory and Autonomic Pain Insensitivity with Anhidrosis, Congenital Sensory Neuropathy, Hereditary Sensory and Autonomic Neuropathies, Hereditary
Scope note in English
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)
See also reference (FX) in Slovak
necitlivosť na bolesť, vrodená
See also reference (FX) in English
Pain Insensitivity, Congenital
Links
(5) - ARTICLES
(1) - MeSH descriptor
(1) - CiBaMed
(8) - BOOKS
subject heading
openseadragon
Number of the records: 1
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