Glycogen storage disease type I risk factors: Difference between revisions
No edit summary |
|||
Line 1: | Line 1: | ||
__NOTOC__ | __NOTOC__ | ||
{{Glycogen storage disease type I}} | {{Glycogen storage disease type I}} | ||
{{CMG}}; {{AE}} | {{CMG}}; {{AE}}{{Anmol}} | ||
{{ | |||
==Overview== | ==Overview== | ||
The most potent risk factor in the development of glycogen storage disease type 1 is a sibling with glycogen storage disease type 1. | |||
==Risk Factors== | ==Risk Factors== |
Revision as of 19:06, 21 November 2017
Glycogen storage disease type I Microchapters |
Differentiating Glycogen storage disease type I from other Diseases |
---|
Diagnosis |
Treatment |
Case Studies |
Glycogen storage disease type I risk factors On the Web |
American Roentgen Ray Society Images of Glycogen storage disease type I risk factors |
Directions to Hospitals Treating Glycogen storage disease type I |
Risk calculators and risk factors for Glycogen storage disease type I risk factors |
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
The most potent risk factor in the development of glycogen storage disease type 1 is a sibling with glycogen storage disease type 1.
Risk Factors
The most potent risk factor in the development of glycogen storage disease type 1 is a sibling with glycogen storage disease type 1.