21-hydroxylase deficiency other diagnostic studies: Difference between revisions

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==Overview==
==Overview==


Immunohistochemical staining of the adrenal-gland may be used for the diagnosis of congenital adrenal hyperplasia due to 21-hydroxylase deficiency and it demonstrates [[hyperplasia]], poorly defined zonation, and intermingling of the [[chromaffin]] and cortical cells.
Immunohistochemical staining of the adrenal-gland may be used for the diagnosis of congenital adrenal hyperplasia due to 21 hydroxylase deficiency and it demonstrates [[hyperplasia]], poorly defined zonation, and intermingling of the [[chromaffin]] and cortical cells.
 
==Other Diagnostic Studies==
==Other Diagnostic Studies==
Immunohistochemical staining of the adrenal-gland may be used in patients with classic 21-hydroxylase deficiency and it demonstrates:
Immunohistochemical staining of the adrenal-gland may be used in patients with classic 21-hydroxylase deficiency and it demonstrates:

Revision as of 17:58, 15 October 2015

Congenital adrenal hyperplasia due to 21-hydroxylase deficiency Microchapters

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

Overview

Immunohistochemical staining of the adrenal-gland may be used for the diagnosis of congenital adrenal hyperplasia due to 21 hydroxylase deficiency and it demonstrates hyperplasia, poorly defined zonation, and intermingling of the chromaffin and cortical cells.

Other Diagnostic Studies

Immunohistochemical staining of the adrenal-gland may be used in patients with classic 21-hydroxylase deficiency and it demonstrates:

  • Poorly defined zonation
  • Intermingling of the chromaffin and cortical cells

References

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