Glycogen storage disease type II CT: Difference between revisions
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Latest revision as of 19:42, 23 January 2018
Glycogen storage disease type II Microchapters |
Differentiating Glycogen storage disease type II from other Diseases |
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Diagnosis |
Treatment |
Case Studies |
Glycogen storage disease type II CT On the Web |
American Roentgen Ray Society Images of Glycogen storage disease type II CT |
Directions to Hospitals Treating Glycogen storage disease type II |
Risk calculators and risk factors for Glycogen storage disease type II CT |
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 CT scan findings associated with glycogen storage disease type 2 (GSD type 2). However, a CT scan may be helpful in the diagnosis of neurological complications of GSD type 2, which include possible widening of the anterior horn of the lateral ventricle and/or peripheral liquor spaces.
CT scan
- There are no CT scan findings associated with glycogen storage disease type 2 (GSD type 2). However, a CT scan may be helpful in the diagnosis of neurological complications of GSD type 2, which include:[1]
- Possible widening of the anterior horn of the lateral ventricle
- Possible widening of the peripheral liquor spaces
References
- ↑ 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.