21-hydroxylase deficiency CT: Difference between revisions
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{{ | {{21-hydroxylase deficiency}} | ||
{{CMG}} {{AE}} {{MJ}} | {{CMG}} {{AE}} {{MJ}} | ||
==Overview== | ==Overview== | ||
Revision as of 14:55, 20 July 2017
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21-hydroxylase deficiency Microchapters |
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Differentiating 21-Hydroxylase Deficiency from other Diseases |
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Diagnosis |
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Treatment |
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Case Studies |
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21-hydroxylase deficiency CT On the Web |
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American Roentgen Ray Society Images of 21-hydroxylase deficiency CT |
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Risk calculators and risk factors for 21-hydroxylase deficiency CT |
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, congenital adrenal hyperplasia due to 21-hydroxylase deficiency is characterized by bilateral symmetric enlargement of the adrenal glands.
CT Scan Findings in Congenital adrenal hyperplasia due to 21-hydroxylase deficiency
On abdominal CT scan, congenital adrenal hyperplasia due to 21-hydroxylase deficiency is characterized by bilateral symmetric enlargement of the adrenal glands.[1]
References
- ↑ 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.