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Diseases

Guillain-Barre Syndrome, Familial

guillain-barre syndrome, familial

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Entity Type
Diseases
Relation Groups
3
Relation Preview
24

Basic Information

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Core Information

Disease Name
Guillain-Barre Syndrome, Familial
Standard Disease Name
guillain-barre syndrome, familial
MeSH Tree
No data
ICD-10
No data

Identifiers

DO ID
No data
MeSH ID
No data
OMIM ID
139393
UMLS ID
C3542501|C0393819|C4083008
HPO ID
No data

Description and Extensions

Description
SNOMEDCT_US_2016_09_01:An inflammatory neuropathy belonging to the clinical spectrum of Guillain-Barré syndrome. The clinical course is divided into three phases. The first phase (lasting a few weeks) has characteristics of rapidly progressive muscle weakness. It is symmetrical and may cause acute neuromuscular paralysis. Sensory disturbances, intense pains, and cramps may also occur. During the second phase (variable duration), symptoms become stable but other manifestations (cardiac arrhythmias, hyper/hypotension and gastric dysmotility) may occur. During the third (recovery) phase, lasting a few months or longer, symptoms slowly regress. Many patients have residual findings (weakness, sensory disturbances, fatigue or pain) for many months or even years. In the majority of cases, an infectious disease precedes the onset of limb weakness, with Campylobacter jejuni infection being the most frequent initiating event.|NCI2016_NICHD_1602D:A subtype of Guillain-Barre Syndrome that targets the myelin sheath, and is characterized by progressive weakness, distal paresthesia and autonomic dysfunction.|NCI2016_02D:An acute inflammatory process affecting the peripheral nervous system and nerve roots. It results in demyelination. It is often caused by an acute viral or bacterial infection.|NCI2016_02D:A subtype of Guillain-Barre syndrome that targets the myelin sheath, and is characterized by progressive weakness, distal paresthesia and autonomic dysfunction.
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