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dysautonómia familiárna

Subject h.	dysautonómia familiárna
Subject h.	Dysautonomia, Familial
Entry terms	neuropatia dedičná senzorická a autonómna, typ III neuropatia dedičná senzitívna a autonómna, typ III HSAN, typ III neuropatia dedičná a autonómna, typ III Rileyov-Dayov syndróm neuropatia dedičná senzorická dominantná, typ III neuropatia dedičná senzitívna dominantná, typ III HSAN (dedičná senzorická a autonómna neuropatia), typ III HSAN (dedičná senzitívna a autonómna neuropatia), typ III HSAN (hereditárna senzorická a autonómna neuropatia), typ III HSAN (hereditárna senzitívna a autonómna neuropatia), typ III HSAN 3 HSAN III HSAN3 HSAN-III neuropatia dedičná senzorická, typ 3 neuropatia hereditárna senzorická, typ 3 neuropatia dedičná senzitívna, typ 3 neuropatia hereditárna senzitívna, typ 3
English X references	HSAN Type III Hereditary-Sensory and Autonomic Neuropathy Type III Neuropathy, Hereditary and Autonomic, Type III Riley-Day Syndrome
Scope note in English	An autosomal disorder of the peripheral and autonomic nervous systems limited to individuals of Ashkenazic Jewish descent. Clinical manifestations are present at birth and include diminished lacrimation, defective thermoregulation, orthostatic hypotension (HYPOTENSION, ORTHOSTATIC), fixed pupils, excessive SWEATING, loss of pain and temperature sensation, and absent reflexes. Pathologic features include reduced numbers of small diameter peripheral nerve fibers and autonomic ganglion neurons. (From Adams et al., Principles of Neurology, 6th ed, p1348; Nat Genet 1993;4(2):160-4)
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