Iranian Journal of Child Neurology

Vol. 6 No. 4 (2012)

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.

 

 

 

 

Keywords:
  • Pompe disease
  • Infantile pompe disease
  • Cardiomyopathy
  • Dried Blood Spot test

How to Cite

ASHRAFI, M. R., & TAVASOLI, A. (2012). Infantile-Onset Pompe Disease. Iranian Journal of Child Neurology, 6(4), 7–9. https://doi.org/10.22037/ijcn.v6i4.3890
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