Glycogen storage disease type I differential diagnosis: Difference between revisions
(Created page with "__NOTOC__ {{Glycogen storage disease type I}} {{CMG}} ==Overview== ==Differentiating Glycogen storage disease type I from other diseases== The differential diagnosis list incl...") |
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__NOTOC__ | __NOTOC__ | ||
{{Glycogen storage disease type I}} | {{Glycogen storage disease type I}} | ||
{{CMG}} | {{CMG}}; {{AE}} | ||
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==Overview== | ==Overview== | ||
==Differentiating Glycogen storage disease type I from other diseases== | ==Differentiating Glycogen storage disease type I from other diseases== | ||
The differential diagnosis list includes [[glycogenoses]] types III and VI, [[fructose 1,6-bisphosphatase]] deficiency, and a few other conditions, but none are likely to produce all of the features of GSD I. | The differential diagnosis list includes [[glycogenoses]] types III and VI, [[fructose 1,6-bisphosphatase]] deficiency, and a few other conditions, but none are likely to produce all of the features of GSD I. | ||
==References== | ==References== | ||
{{reflist|2}} | {{reflist|2}} | ||
[[Category:Endocrinology]] | [[Category:Endocrinology]] | ||
[[Category:Hepatology]] | [[Category:Hepatology]] | ||
[[Category:Gastroenterology]] | [[Category:Gastroenterology]] | ||
{{WS}} | |||
{{WH}} | |||
Revision as of 15:48, 19 July 2016
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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief:
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Overview
Differentiating Glycogen storage disease type I from other diseases
The differential diagnosis list includes glycogenoses types III and VI, fructose 1,6-bisphosphatase deficiency, and a few other conditions, but none are likely to produce all of the features of GSD I.