21-hydroxylase deficiency ultrasound: Difference between revisions

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== References ==
== References ==
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Revision as of 14:40, 14 November 2017

Congenital adrenal hyperplasia main page

21-hydroxylase deficiency Microchapters

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Differentiating 21-Hydroxylase Deficiency from other Diseases

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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 ultrasound, 21-hydroxylase deficiency is characterized by enlarged, wrinkled, and cerebriform adrenal glands. Testicular masses may be seen in the setting of classical disease.

Ultrasound Findings in 21-hydroxylase deficiency

Ultrasound findings in patients with 21 hydroxylase deficiency are:[1][2]

References

  1. Congenital adrenal hyperplasia. Dr Henry Knipe and Dr M Venkatesh . Radiopaedia.org 2015.http://radiopaedia.org/articles/congenital-adrenal-hyperplasia
  2. Teixeira SR, Elias PC, Andrade MT, Melo AF, Elias Junior J (2014). "The role of imaging in congenital adrenal hyperplasia". Arq Bras Endocrinol Metabol. 58 (7): 701–8. PMID 25372578.

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