11β-hydroxylase deficiency CT: Difference between revisions

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__NOTOC__
__NOTOC__
{{Congenital adrenal hyperplasia due to 11β-hydroxylase deficiency}}
{{11β-hydroxylase deficiency}}
{{CMG}} {{AE}} {{AAM}}
{{CMG}} {{AE}} {{MJ}}
==Overview==
==Overview==
On abdominal [[CT scan]], congenital adrenal hyperplasia due to 11β-hydroxylase deficiency is characterized by bilateral symmetric enlargement of the [[adrenal glands]].
On abdominal [[CT scan]], 11β-hydroxylase deficiency is characterized by bilateral symmetric enlargement of the [[adrenal glands]].
 
==CT Scan==
==CT Scan Findings in Congenital adrenal hyperplasia due to 21-hydroxylase deficiency==
On abdominal [[CT scan]], 11β-hydroxylase deficiency is characterized by bilateral symmetric enlargement of the [[adrenal glands]].<ref name="pmid28707538">{{cite journal |vauthors=Agrons M, Jensen CT, Habra MA, Menias CO, Shaaban AM, Wagner-Bartak NA, Roman-Colon AM, Elsayes KM |title=Adrenal Cortical Hyperplasia: Diagnostic Workup, Subtypes, Imaging Features and Mimics |journal=Br J Radiol |volume= |issue= |pages=20170330 |year=2017 |pmid=28707538 |doi=10.1259/bjr.20170330 |url=}}</ref>
On abdominal [[CT scan]], congenital adrenal hyperplasia due to 11β-hydroxylase deficiency is characterized by bilateral symmetric enlargement of the [[adrenal glands]].
 
== References ==
== References ==
{{Reflist|2}}
{{Reflist|2}}
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Latest revision as of 16:59, 7 August 2017

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

Overview

On abdominal CT scan, 11β-hydroxylase deficiency is characterized by bilateral symmetric enlargement of the adrenal glands.

CT Scan

On abdominal CT scan, 11β-hydroxylase deficiency is characterized by bilateral symmetric enlargement of the adrenal glands.[1]

References

  1. Agrons M, Jensen CT, Habra MA, Menias CO, Shaaban AM, Wagner-Bartak NA, Roman-Colon AM, Elsayes KM (2017). "Adrenal Cortical Hyperplasia: Diagnostic Workup, Subtypes, Imaging Features and Mimics". Br J Radiol: 20170330. doi:10.1259/bjr.20170330. PMID 28707538.