Guillain-Barre Syndrome, Familial (GBS)

Alias:

Acute Inflammatory Demyelinating Polyradiculoneuropathy

Acute Inflammatory Demyelinating Polyneuropathy

Aidp

Gbs

Guillain-Barre Syndrome, Acute Inflammatory Demyelinating Polyradiculoneuropathic Form

Gbs, Acute Inflammatory Demyelinating Polyradiculoneuropathic Form

Polyneuropathy, Inflammatory Demyelinating, Acute

Acute Idiopathic Demyelinating Polyneuropathy

Polyneuropathy, Inflammatory Demyelinating

Inflammatory Demyelinating Polyneuropathy

Neuropathy, Inflammatory Demyelinating

Acute Encephalomyeloradiculoneuritis

Acute Inflammatory Polyneuropathy

Acute Ascending Paralysis

Chronic Polyradiculopathy

Guillain-Barré Syndrome

Guillain Barre Syndrome

Landry's Paralysis

Landry's Disease

Idp

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Basic Information

Medical Symptom

Gene & Mutation

Related Drugs

Disease Model

References Literature

Guillain-Barre Syndrome, Familial, also known as acute inflammatory demyelinating polyradiculoneuropathy, is related to guillain-barre syndrome and miller fisher syndrome. An important gene associated with Guillain-Barre Syndrome, Familial is PMP22 (Peripheral Myelin Protein 22). The drugs Prednisolone and Prednisolone acetate have been mentioned in the context of this disorder. Affiliated tissues include brain and spinal cord, and related phenotypes are acute demyelinating polyneuropathy and hyporeflexia

Related ID：

MALACARDS：GLL037

OMIM：139393

ICD11：1196874419