gq1b-ganglioside and Inappropriate-ADH-Syndrome

gq1b-ganglioside has been researched along with Inappropriate-ADH-Syndrome* in 1 studies

Other Studies

1 other study(ies) available for gq1b-ganglioside and Inappropriate-ADH-Syndrome

Article	Year
[A case of Guillain-Barré syndrome complicated with severe autonomic failure and presented elevated anti-GD1b and anti-GQ1b antibody]. Rinsho shinkeigaku = Clinical neurology, 2002, Volume: 42, Issue:1 We report a 30-year-old woman who presented symptoms of oropharyngeal palsy and glove-stocking type sensory disturbance followed by acute cerebellar ataxia, the syndrome of inappropriate secretion of antidiuretic hormone (SIADH), gastroenteric symptoms, urinary disturbance and orthostatic hypotension. She did not have any preceding infection. She was diagnosed as having Guillain-Barré syndrome with autonomic failure. Autonomic failure such as sinus tachycardia and nocturnal ventricular arrhythmia in addition to motor and sensory dysfunction was palliated by immunoadsorption. During the course of her illness, there were elevations of antiganglioside antibodies to GT1a and GQ1b in the IgG subclass, and to GD1b and GQ1b in the IgM subclass. The elevation of anti-GD1b antibody and anti-GQ1b antibody may be pathologically related to autonomic failure, cerebellar ataxia and SIADH. Topics: Adult; Autoantibodies; Autonomic Nervous System Diseases; Cerebellar Ataxia; Female; Gangliosides; Guillain-Barre Syndrome; Humans; Inappropriate ADH Syndrome	2002

Article

Year

[A case of Guillain-Barré syndrome complicated with severe autonomic failure and presented elevated anti-GD1b and anti-GQ1b antibody].

Rinsho shinkeigaku = Clinical neurology, 2002, Volume: 42, Issue:1

We report a 30-year-old woman who presented symptoms of oropharyngeal palsy and glove-stocking type sensory disturbance followed by acute cerebellar ataxia, the syndrome of inappropriate secretion of antidiuretic hormone (SIADH), gastroenteric symptoms, urinary disturbance and orthostatic hypotension. She did not have any preceding infection. She was diagnosed as having Guillain-Barré syndrome with autonomic failure. Autonomic failure such as sinus tachycardia and nocturnal ventricular arrhythmia in addition to motor and sensory dysfunction was palliated by immunoadsorption. During the course of her illness, there were elevations of antiganglioside antibodies to GT1a and GQ1b in the IgG subclass, and to GD1b and GQ1b in the IgM subclass. The elevation of anti-GD1b antibody and anti-GQ1b antibody may be pathologically related to autonomic failure, cerebellar ataxia and SIADH.

Topics: Adult; Autoantibodies; Autonomic Nervous System Diseases; Cerebellar Ataxia; Female; Gangliosides; Guillain-Barre Syndrome; Humans; Inappropriate ADH Syndrome

2002