Hereditary Sensory and Autonomic Neuropathies [dědičné senzorické a autonomní neuropatie]

topical
26
Terms

dědičná senzorická a autonomní neuropatie, typ 1
dědičná senzorická a autonomní neuropatie, typ 2
dědičná senzorická a autonomní neuropatie, typ 4
dědičná senzorická a autonomní neuropatie, typ 5
dědičná senzorická a autonomní neuropatie, typ IV
dědičná senzorická neuropatie
dědičná senzorická radikulární neuropatie
familiární dysautonomie, typ 2
Giaccai syndrom
hereditární senzorické a autonomní neuropatie
HSAN - typ IV
kongenitální insenzitivita k bolesti s anhidrózou
vrozená necitlivost k bolesti s anhidrózou
vrozená necitlivost na bolest s anhidrózou

 

Acroosteolysis, Giaccai Type
Acroosteolysis, Neurogenic
Congenital Insensitivity to Pain with Anhidrosis
Familial Dysautonomia, Type 2
Familial Dysautonomia, Type II
Giaccai Type Acroosteolysis
Hereditary Sensory and Autonomic Neuropathy 4
Hereditary Sensory And Autonomic Neuropathy IV
Hereditary Sensory and Autonomic Neuropathy Type 1
Hereditary Sensory and Autonomic Neuropathy Type 2
Hereditary Sensory and Autonomic Neuropathy Type I
Hereditary Sensory and Autonomic Neuropathy Type II
Hereditary Sensory and Autonomic Neuropathy Type IV
Hereditary Sensory and Autonomic Neuropathy Type V
Hereditary Sensory and Autonomic Neuropathy, Type 4
Hereditary Sensory and Autonomic Neuropathy, Type 5
Hereditary Sensory Autonomic Neuropathy, Type 1
Hereditary Sensory Autonomic Neuropathy, Type 2
Hereditary Sensory Autonomic Neuropathy, Type 4
Hereditary Sensory Autonomic Neuropathy, Type 5
Hereditary Sensory Neuropathy Type 1
Hereditary Sensory Neuropathy Type I
Hereditary Sensory Neuropathy Type Ia
Hereditary Sensory Radicular Neuropathy
Hereditary Sensory Radicular Neuropathy, Recessive Form
HSAN
HSAN (Hereditary Sensory Autonomic Neuropathy)
HSAN 1
HSAN 4
HSAN 5
HSAN I
HSAN IV
HSAN Type I
HSAN Type II
HSAN Type IV
HSAN Type V
HSAN V
HSAN2
HSAN5
HSANII
HSN Type I
HSN Type II
Insensitivity to Pain with Anhidrosis, Congenital
Insensitivity to Pain, Congenital, with Anhidrosis
Neurogenic Acroosteolysis
Neuropathies, Hereditary Sensory and Autonomic
Neuropathy Hereditary Sensory and Autonomic Type 1
Neuropathy Hereditary Sensory Radicular, Autosomal Dominant
Neuropathy, Congenital Sensory
Neuropathy, Congenital Sensory, with Anhidrosis
Neuropathy, Hereditary Sensory And Autonomic, Type I
Neuropathy, Hereditary Sensory And Autonomic, Type V
Neuropathy, Hereditary Sensory Radicular, Autosomal Dominant
Neuropathy, Hereditary Sensory Radicular, Autosomal Recessive
Neuropathy, Hereditary Sensory, Type I
Neuropathy, Progressive Sensory, Of Children
Pain Insensitivity with Anhidrosis, Congenital
Sensory and Autonomic Neuropathies, Hereditary
Sensory Neuropathy, Hereditary

Persistent link   https://www.medvik.cz/link/D009477
Definition

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)

Annotation
do not confuse with HEREDITARY SENSORY AND MOTOR NEUROPATHY; note entry terms for HSAN types: HSAN TYPE III see DYSAUTONOMIA, FAMILIAL is also available
DUI
D009477 MeSH Browser
CUI
M0014743
Previous indexing
Peripheral Nerve Diseases (1966-1978); Peripheral Nerves (1966-1978); Sensation (1966-1978)
History note
2000(1989); use NEUROPATHY, HEREDITARY SENSORY 1979-1988
Public note
2000; see NEUROPATHIES, HEREDITARY SENSORY AND AUTONOMIC 1989-1999; see NEUROPATHY, HEREDITARY SENSORY 1979-1988

C Diseases
C10.500.250.309 Dysautonomia, Familial 7
C10.500.450 Hydranencephaly 3
C10.500.680 Neural Tube Defects 77
C10.574.500.024 Alexander Disease 6
C10.574.500.300 Canavan Disease 9
C10.574.500.362 Cockayne Syndrome 4
C10.574.500.493.250 Dysautonomia, Familial 7
C10.574.500.497 Huntington Disease 322
C10.574.500.529 Lafora Disease 1
C10.574.500.545 Myotonia Congenita 17
C10.574.500.547 Myotonic Dystrophy 94
C10.574.500.549 Neurofibromatoses 28
C10.574.500.850 Tourette Syndrome 86
C10.574.500.865 Tuberous Sclerosis 141
C10.668.829.800 Polyneuropathies 342
C10.668.829.800.050 Alcoholic Neuropathy 18
C10.668.829.800.175.250 Dysautonomia, Familial 7
C10.668.829.800.662 Paraneoplastic Polyneuropathy 14
C10.668.829.800.700 POEMS Syndrome 34
C10.668.829.800.750 Polyradiculoneuropathy 68
C10.668.829.800.875 Tangier Disease 3
C16.131.666.205 Dandy-Walker Syndrome 6
C16.131.666.310.309 Dysautonomia, Familial 7
C16.131.666.450 Hydranencephaly 3
C16.131.666.680 Neural Tube Defects 77
C16.131.666.763 Optic Nerve Hypoplasia 1
C16.320.400.024 Alexander Disease 6
C16.320.400.150 Canavan Disease 9
C16.320.400.200 Cockayne Syndrome 4
C16.320.400.415.309 Dysautonomia, Familial 7
C16.320.400.430 Huntington Disease 322
C16.320.400.480 Lafora Disease 1
C16.320.400.540 Myotonia Congenita 17
C16.320.400.542 Myotonic Dystrophy 94
C16.320.400.550 Neuroacanthocytosis 6
C16.320.400.560 Neurofibromatoses 28
C16.320.400.820 Tourette Syndrome 86
C16.320.400.880 Tuberous Sclerosis 141