Glucose-6-phosphate dehydrogenase deficiency CT: Difference between revisions

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Latest revision as of 14:31, 17 October 2018

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

There are no CT scan findings associated with Glucose-6-phosphate dehydrogenase deficiency.

There are no CT scan findings associated with Glucose-6-phosphate dehydrogenase deficiency.

@@ Line 1: / Line 1: @@
+__NOTOC__
 {{Glucose-6-phosphate dehydrogenase deficiency}}
-{{CMG}}; '''Associate Editor(s)-In-Chief:''' [[Priyamvada Singh|Priyamvada Singh, M.D.]] [mailto:psingh@perfuse.org]
+{{CMG}}; {{AE}}{{MA}}
 ==Overview==
-'''Glucose-6-phosphate dehydrogenase (G6PD) deficiency''' is an [[Sex-linked|X-linked recessive]] [[hereditary disease]] featuring abnormally low levels of the [[G6PD]] enzyme, which plays an important role in [[red blood cell]] function. Individuals with the disease may exhibit non-immune [[hemolytic anemia]] in response to a number of causes. It is closely linked to '''[[favism]]''', a disorder characterized by a hemolytic reaction to consumption of [[Vicia faba|broad bean]]s, with a name derived from the [[Italian language|Italian]] name of the broad bean (''fava''). Sometimes the name, [[favism]], is alternatively used to refer to the enzyme
+There are no CT scan findings associated with Glucose-6-phosphate dehydrogenase deficiency.
-deficiency as a whole.
+==CT scan==
+There are no CT scan findings associated with Glucose-6-phosphate dehydrogenase deficiency.
 ==References==
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+{{Reflist|2}}
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-{{WikiDoc Sources}}
-[[Category:Disease]]
+{{WH}}
-[[Category:Hematology]]
+{{WS}}
-[[Category:Mature chapter]]
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