Skip to main content

Search from vocabulary

Content language

Concept information

Pathological Conditions, Signs and Symptoms > Pathologic Processes > Disease Attributes > Chronic Disease > Polyradiculoneuropathy, Chronic Inflammatory Demyelinating
Immune System Diseases > Autoimmune Diseases > Autoimmune Diseases of the Nervous System > Polyradiculoneuropathy > Polyradiculoneuropathy, Chronic Inflammatory Demyelinating
Nervous System Diseases > Autoimmune Diseases of the Nervous System > Polyradiculoneuropathy > Polyradiculoneuropathy, Chronic Inflammatory Demyelinating
Nervous System Diseases > Demyelinating Diseases > Polyradiculoneuropathy > Polyradiculoneuropathy, Chronic Inflammatory Demyelinating

Preferred term

Polyradiculoneuropathy, Chronic Inflammatory Demyelinating  

Type

  • Topical Descriptor

Entry terms

  • Chronic Inflammatory Demyelinating Polyradiculoneuropathy
  • Chronic Inflammatory Polyradiculoneuropathies
  • Chronic Inflammatory Polyradiculoneuropathy
  • Chronic Inflammatory Polyradiculopathies
  • Chronic Inflammatory Polyradiculopathy
  • CIDP
  • Inflammatory Polyradiculoneuropathies, Chronic
  • Inflammatory Polyradiculoneuropathy, Chronic
  • Inflammatory Polyradiculopathies, Chronic
  • Inflammatory Polyradiculopathy, Chronic
  • Polyneuropathy, Inflammatory Demyelinating, Chronic
  • Polyradiculoneuropathies, Chronic Inflammatory
  • Polyradiculoneuropathy, Chronic Inflammatory
  • Polyradiculopathies, Chronic Inflammatory
  • Polyradiculopathy, Chronic Inflammatory

Note

  • do not confuse entry term CHRONIC INFLAMMATORY POLYRADICULONEUROPATHY with POLYRADICULONEUROPATHY, ACUTE INFLAMMATORY see GUILLAIN-BARRE SYNDROME

Scope note

  • A slowly progressive autoimmune demyelinating disease of peripheral nerves and nerve roots. Clinical manifestations include weakness and sensory loss in the extremities and enlargement of peripheral nerves. The course may be relapsing-remitting or demonstrate a step-wise progression. Protein is usually elevated in the spinal fluid and cranial nerves are typically spared. GUILLAIN-BARRE SYNDROME features a relatively rapid progression of disease which distinguishes it from this condition. (Adams et al., Principles of Neurology, 6th ed, p1337)

History note

  • 2000

In other languages

URI

http://www.yso.fi/onto/mesh/D020277

Download this concept:

RDF/XML TURTLE JSON-LD Created 11/5/99, last modified 3/12/21