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acute inflammatoire demyeliniserende polyradiculoneuropathie (aandoening)
acute inflammatoire demyeliniserende polyradiculoneuropathie
acute inflammatoire demyeliniserende polyradiculoneuropathische vorm van syndroom van Guillain-Barré
acute inflammatoire demyeliniserende polyradiculoneuropathische vorm van Guillain-Barré-syndroom
AIDP
Acute inflammatory demyelinating polyradiculoneuropathy
Guillain-Barré syndrome acute inflammatory demyelinating polyradiculoneuropathic form
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.
Id716723000
StatusPrimitive
Associated morphologydemyelinisatie
Finding sitestructuur van perifere zenuw
Pathological processauto-immuunproces
Associated morphologyinflammatoire morfologie
Finding sitestructuur van perifere zenuw
Pathological processauto-immuunproces
SNOMED CT to Orphanet simple map98916
SNOMED CT to ICD-10 extended map
TargetG61.0
RuleTRUE
AdviceALWAYS G61.0
CorrelationSNOMED CT source code to target map code correlation not specified