Neuromyelitis optica in marfan syndrome

المؤلف

al-Shamrani, Fawziyah Jabar

المصدر

Bahrain Medical Bulletin

العدد

المجلد 36، العدد 1 (31 مارس/آذار 2014)، ص ص. 1-4، 4ص.

الناشر

مستشفى الملك حمد الجامعي

تاريخ النشر

2014-03-31

دولة النشر

البحرين

عدد الصفحات

4

التخصصات الرئيسية

الطب البشري

الموضوعات

الملخص EN

Neuromyelitis optica (NMO) is one of the differential diagnoses that should be considered in a patient with unilateral or bilateral loss of vision.

It should be evaluated by history, examination, serological testing and neuroimaging studies.

We report a case of a 39-year-old gentleman who was known to have Marfan's syndrome and presented with progressive loss of vision in one eye followed by the other one within one month.

Neurological examination showed bilateral optic neuritis (ON) with optic atrophy and unilateral upper motor neuron signs.

CSF analysis was positive for NMO-IgG; MRI of the brain and spine showed enhancement in both optic nerves pathways and the optic chiasm with normal spine appearance.

نمط استشهاد جمعية علماء النفس الأمريكية (APA)

al-Shamrani, Fawziyah Jabar. 2014. Neuromyelitis optica in marfan syndrome. Bahrain Medical Bulletin،Vol. 36, no. 1, pp.1-4.
https://search.emarefa.net/detail/BIM-603465

نمط استشهاد الجمعية الأمريكية للغات الحديثة (MLA)

al-Shamrani, Fawziyah Jabar. Neuromyelitis optica in marfan syndrome. Bahrain Medical Bulletin Vol. 36, no. 1 (Mar. 2014), pp.1-4.
https://search.emarefa.net/detail/BIM-603465

نمط استشهاد الجمعية الطبية الأمريكية (AMA)

al-Shamrani, Fawziyah Jabar. Neuromyelitis optica in marfan syndrome. Bahrain Medical Bulletin. 2014. Vol. 36, no. 1, pp.1-4.
https://search.emarefa.net/detail/BIM-603465

نوع البيانات

مقالات

لغة النص

الإنجليزية

الملاحظات

Includes bibliographical references

رقم السجل

BIM-603465