Glycogen storage disease type II x ray

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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Anmol Pitliya, M.B.B.S. M.D.[2]

Overview

There are no X-ray findings associated with glycogen storage disease type 2 (GSD type 2). However, an X-ray may be helpful in the diagnosis of the cardiac complication of GSD type 2, which include cardiomegaly.

X Ray

  • There are no X-ray findings associated with glycogen storage disease type 2 (GSD type 2). However, an X-ray may be helpful in the diagnosis of the cardiac complication of GSD type 2, which include:[1][2]

References

  1. van den Hout HM, Hop W, van Diggelen OP, Smeitink JA, Smit GP, Poll-The BT; et al. (2003). "The natural course of infantile Pompe's disease: 20 original cases compared with 133 cases from the literature". Pediatrics. 112 (2): 332–40. PMID 12897283.
  2. ACMG Work Group on Management of Pompe Disease. Kishnani PS, Steiner RD, Bali D, Berger K, Byrne BJ; et al. (2006). "Pompe disease diagnosis and management guideline". Genet Med. 8 (5): 267–88. doi:10.109701.gim.0000218152.87434.f3 Check |doi= value (help). PMC 3110959. PMID 16702877.



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