Miller-fisher syndrome : a variant of Guillain-Barre syndrome

المؤلف

Jadah, Rafat Hammad Surur

المصدر

Bahrain Medical Bulletin

العدد

المجلد 41، العدد 3 (30 سبتمبر/أيلول 2019)، ص ص. 190-191، 2ص.

الناشر

مستشفى الملك حمد الجامعي

تاريخ النشر

2019-09-30

دولة النشر

البحرين

عدد الصفحات

2

التخصصات الرئيسية

الطب البشري

الموضوعات

الملخص EN

Guillain-Barre syndrome (GBS) is a rare neurological condition affecting all ages.

It is rare in pediatric population; the disease is preceded by viral or bacterial infection.

GBS present as a rapid onset ascending paralysis with pain and sensory impairment.

Miller Fisher syndrome is a rare but most recognized variant of GBS; it presents by the classical triad of symptoms: ataxic gait, absence of reflexes and ophthalmoplegia.

A healthy six-year-old boy, not known to have any medical illnesses, presented with the classical triad of symptoms after ten days’ history of gastroenteritis.

Ganglioside GQ1B (IgG, IgM) antibodies were markedly elevated and the patient was started immediately on intravenous immunoglobulin (IVIG).

After a few days, the patient showed marked improvement in gait with no further deterioration in clinical condition.

نمط استشهاد جمعية علماء النفس الأمريكية (APA)

Jadah, Rafat Hammad Surur. 2019. Miller-fisher syndrome : a variant of Guillain-Barre syndrome. Bahrain Medical Bulletin،Vol. 41, no. 3, pp.190-191.
https://search.emarefa.net/detail/BIM-896292

نمط استشهاد الجمعية الأمريكية للغات الحديثة (MLA)

Jadah, Rafat Hammad Surur. Miller-fisher syndrome : a variant of Guillain-Barre syndrome. Bahrain Medical Bulletin Vol. 41, no. 3 (Sep. 2019), pp.190-191.
https://search.emarefa.net/detail/BIM-896292

نمط استشهاد الجمعية الطبية الأمريكية (AMA)

Jadah, Rafat Hammad Surur. Miller-fisher syndrome : a variant of Guillain-Barre syndrome. Bahrain Medical Bulletin. 2019. Vol. 41, no. 3, pp.190-191.
https://search.emarefa.net/detail/BIM-896292

نوع البيانات

مقالات

لغة النص

الإنجليزية

الملاحظات

Includes bibliographical references : p. 191

رقم السجل

BIM-896292