Infantile-Onset Pompe Disease
Iranian Journal of Child Neurology,
Vol. 6 No. 4 (2012),
30 December 2012
,
Page 7-9
https://doi.org/10.22037/ijcn.v6i4.3890
Abstract
How to Cite this Article: Ashrafi MR, Tavasoli AR. Infantile-Onset Pompe Disease. Iran J Child Neurol Autumn 2012; 6:4(suppl. 1):7-9.
Pls see PDF.
References:
1. Kishnani PS, Steiner RD. Pompe disease diagnosis and management guidelines. American J med genetic. 2006 .Vol; 8; no5.
2. Case SE, Beckemyer AA. Infantile pompe disease on ERT-Updateonclinicalpresentation,musculoskeletal management, and Exercise considerations. American J med genetic.160C:69-79(2012).
3. Rocco MD,Buzzi D. Glycogen storage disease type II:clinical overview. Acta myologica. 2007; XXVI; P.42-44.
4. Fenichel GM.Clinical pediatric neurology. Sixth edition.2009; p.174,188.
5.Swaiman KF, Ashwal S. Swaimans’ pediatric neurology. Fifth edition .2012 .Vol.1,p.378-380.
- Pompe disease
- Infantile pompe disease
- Cardiomyopathy
- Dried Blood Spot test
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