Spinal muscular atrophy : non-curative disease

المؤلفون المشاركون

Dunne, Kevin Patrick
al-Sada, Dhabya Abd al-Aziz

المصدر

Bahrain Medical Bulletin

العدد

المجلد 38، العدد 4 (31 ديسمبر/كانون الأول 2016)، ص ص. 233-235، 3ص.

الناشر

مستشفى الملك حمد الجامعي

تاريخ النشر

2016-12-31

دولة النشر

البحرين

عدد الصفحات

3

التخصصات الرئيسية

الطب البشري

الملخص EN

A one-month-old baby girl with spinal muscular atrophy type 1 with generalized muscle weakness is presented.

She was fully investigated and diagnosed with spinal muscular atrophy type 1.

She was managed conservatively and with supportive treatment.

She died at the age of 13 months.

Spinal Muscular Atrophy (SMA) is a non-curative disease with a wide degree of clinical and genetic heterogeneity that we must take into consideration because of the serious prognosis.

It targets the muscles which result in weakness and atrophy.

Several therapeutic approaches have been proposed and investigated.

They are focused on increasing the availability of Survival of Motor Neuron (SMN) protein which has been found effective when tried in animal modelling studies.

نمط استشهاد جمعية علماء النفس الأمريكية (APA)

al-Sada, Dhabya Abd al-Aziz& Dunne, Kevin Patrick. 2016. Spinal muscular atrophy : non-curative disease. Bahrain Medical Bulletin،Vol. 38, no. 4, pp.233-235.
https://search.emarefa.net/detail/BIM-766318

نمط استشهاد الجمعية الأمريكية للغات الحديثة (MLA)

al-Sada, Dhabya Abd al-Aziz& Dunne, Kevin Patrick. Spinal muscular atrophy : non-curative disease. Bahrain Medical Bulletin Vol. 38, no. 4 (Dec. 2016), pp.233-235.
https://search.emarefa.net/detail/BIM-766318

نمط استشهاد الجمعية الطبية الأمريكية (AMA)

al-Sada, Dhabya Abd al-Aziz& Dunne, Kevin Patrick. Spinal muscular atrophy : non-curative disease. Bahrain Medical Bulletin. 2016. Vol. 38, no. 4, pp.233-235.
https://search.emarefa.net/detail/BIM-766318

نوع البيانات

مقالات

لغة النص

الإنجليزية

الملاحظات

Includes bibliographical references : p. 235

رقم السجل

BIM-766318