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A Case Report of Sensory Guillain-Barré Syndrome with Prominent Autonomic Dysfunction in a Systemic Lupus Erythematosus Patient / 대한신경근육질환학회지
Article in Ko | WPRIM | ID: wpr-968174
Responsible library: WPRO
ABSTRACT
Sensory Guillain-Barré syndrome (GBS) is a rare heterogeneous subgroup of GBS characterized by the primary involvement of sensory neurons resulting in a distinctive clinical presentation. Sensory GBS usually occurs with acute and monophasic sensory symptoms, and no or minimal muscle weakness. Sensory GBS patient show hypo- or areflexia, distal paresthesia, and normal cerebrospinal fluid finding or albumino-cytologic dissociation which are suggesting that these conditions are a GBS variant. Autonomic dysfunctions have rarely been reported in sensory GBS patient presenting with postural hypotension, abnormal heart rate response to respiration. In this case, we demonstrate a patient with autonomic symptoms dominant sensory GBS in systemic lupus erythematosus.
Full text: 1 Index: WPRIM Language: Ko Journal: Korean Journal of Neuromuscular Disorders Year: 2022 Type: Article
Full text: 1 Index: WPRIM Language: Ko Journal: Korean Journal of Neuromuscular Disorders Year: 2022 Type: Article