Hirayama Disease: A Rare Disease with Unusual Features

المؤلفون المشاركون

Anuradha, S.
Fanai, Vanlalmalsawmdawngliana

المصدر

Case Reports in Neurological Medicine

العدد

المجلد 2016، العدد 2016 (31 ديسمبر/كانون الأول 2016)، ص ص. 1-4، 4ص.

الناشر

Hindawi Publishing Corporation

تاريخ النشر

2016-12-21

دولة النشر

مصر

عدد الصفحات

4

التخصصات الرئيسية

الطب البشري

الملخص EN

Hirayama disease, also known as monomelic amyotrophy (MMA), is a rare cervical myelopathy that manifests itself as a self-limited, asymmetrical, slowly progressive atrophic weakness of the forearms and hands predominantly in young males.

The forward displacement of the posterior dura of the lower cervical dural canal during neck flexion has been postulated to lead to lower cervical cord atrophy with asymmetric flattening.

We report a case of Hirayama disease in a 25-year-old Indian man presenting with gradually progressive asymmetrical weakness and wasting of both hands and forearms along with unusual features of autonomic dysfunction and upper motor neuron lesion.

نمط استشهاد جمعية علماء النفس الأمريكية (APA)

Anuradha, S.& Fanai, Vanlalmalsawmdawngliana. 2016. Hirayama Disease: A Rare Disease with Unusual Features. Case Reports in Neurological Medicine،Vol. 2016, no. 2016, pp.1-4.
https://search.emarefa.net/detail/BIM-1101300

نمط استشهاد الجمعية الأمريكية للغات الحديثة (MLA)

Anuradha, S.& Fanai, Vanlalmalsawmdawngliana. Hirayama Disease: A Rare Disease with Unusual Features. Case Reports in Neurological Medicine No. 2016 (2016), pp.1-4.
https://search.emarefa.net/detail/BIM-1101300

نمط استشهاد الجمعية الطبية الأمريكية (AMA)

Anuradha, S.& Fanai, Vanlalmalsawmdawngliana. Hirayama Disease: A Rare Disease with Unusual Features. Case Reports in Neurological Medicine. 2016. Vol. 2016, no. 2016, pp.1-4.
https://search.emarefa.net/detail/BIM-1101300

نوع البيانات

مقالات

لغة النص

الإنجليزية

الملاحظات

Includes bibliographical references

رقم السجل

BIM-1101300