Congenital adrenal hyperplasia classification: Difference between revisions

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==Classification==
==Classification==
The most common cause of congenital adrenal hyperplasia worldwide, accounting for more than 90 percent of cases, is 21-hydroxylase deficiency.<ref name="pmid10857554">{{cite journal |vauthors=White PC, Speiser PW |title=Congenital adrenal hyperplasia due to 21-hydroxylase deficiency |journal=Endocr. Rev. |volume=21 |issue=3 |pages=245–91 |year=2000 |pmid=10857554 |doi=10.1210/edrv.21.3.0398 |url=}}</ref>
21-hydroxylase deficiency, genetic defects: CYP21A2
11β-hydroxylase deficiency, genetic defects: CYP11B1
17α-hydroxylase/ 17,20-lyase deficiency, genetic defects: CYP17A1
3β-hydroxy-steroid dehydrogenase type 2 deficiency,genetic defects: HSD3B2
P450 oxidoreductase deficiency, genetic defects: POR
Hexose-6-phosphate-dehydrogenase deficiency (apparent cortisone reductase deficiency [ACRD]) 
PAPSS2 deficiency (apparent dehydroepiandrosterone [DHEA] sulfotransferase deficiency
Lipoid adrenal hyperplasia, genetic defects: StAR
Cholesterol side chain cleavage enzyme deficiency, genetic defects: CYP11A1


==References==
==References==

Revision as of 19:26, 6 July 2017

Congenital adrenal hyperplasia main page

Overview

Classification

21-hydroxylase deficiency
11β-hydroxylase deficiency
17 alpha-hydroxylase deficiency
3 beta-hydroxysteroid dehydrogenase deficiency
Cytochrome P450-oxidoreductase (POR) deficiency (ORD)
Lipoid congenital adrenal hyperplasia

Differential Diagnosis

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

Overview

Classification

The most common cause of congenital adrenal hyperplasia worldwide, accounting for more than 90 percent of cases, is 21-hydroxylase deficiency.[1]


21-hydroxylase deficiency, genetic defects: CYP21A2

11β-hydroxylase deficiency, genetic defects: CYP11B1

17α-hydroxylase/ 17,20-lyase deficiency, genetic defects: CYP17A1

3β-hydroxy-steroid dehydrogenase type 2 deficiency,genetic defects: HSD3B2

P450 oxidoreductase deficiency, genetic defects: POR

Hexose-6-phosphate-dehydrogenase deficiency (apparent cortisone reductase deficiency [ACRD])

PAPSS2 deficiency (apparent dehydroepiandrosterone [DHEA] sulfotransferase deficiency

Lipoid adrenal hyperplasia, genetic defects: StAR

Cholesterol side chain cleavage enzyme deficiency, genetic defects: CYP11A1

References

  1. White PC, Speiser PW (2000). "Congenital adrenal hyperplasia due to 21-hydroxylase deficiency". Endocr. Rev. 21 (3): 245–91. doi:10.1210/edrv.21.3.0398. PMID 10857554.


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