Congenital adrenal hyperplasia: Difference between revisions

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[[Image:DHEA1_svg.png|thumb|center|800px|Production of DHEA from Cholesterol. ([[Cortisol]] is a [[glucocorticoid]].)]]
[[Image:DHEA1_svg.png|thumb|center|800px|Production of DHEA from Cholesterol. ([[Cortisol]] is a [[glucocorticoid]].)]]
===Classification===
===Classification===
* [[Congenital adrenal hyperplasia due to 21-hydroxylase deficiency]]
{{Familytree/start}}
* [[Lipoid congenital adrenal hyperplasia]]
{{Familytree|boxstyle=background: #E0FFFF;| | | | | | | | | | | | | | A01 | | | | | | | | | | | | | | | | | | |A01= Congenital Adrenal Hyperplasia}}
* [[Congenital adrenal hyperplasia due to 17 alpha-hydroxylase deficiency|Congenital adrenal hyperplasia due to 17α-hydroxylase deficiency]]
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* [[Congenital adrenal hyperplasia due to 3 beta-hydroxysteroid dehydrogenase deficiency|Congenital adrenal hyperplasia due to 3β-hydroxysteroid dehydrogenase deficiency]]
{{Familytree|boxstyle=background: #E0FFFF;| | | | B01 | | | B02 | | | | | | | | B03 | | | B04 | | B05 | | | | | | | |B01= [[Lipoid congenital adrenal hyperplasia]]|B02= [[Congenital adrenal hyperplasia due to 21-hydroxylase deficiency]]|B03= [[Congenital adrenal hyperplasia due to 17 alpha-hydroxylase deficiency]]|B04= [[Congenital adrenal hyperplasia due to 3 beta-hydroxysteroid dehydrogenase deficiency]]|B05= [[Congenital adrenal hyperplasia due to 11 beta-hydroxysteroid dehydrogenase deficiency]]}}
* [[Congenital adrenal hyperplasia due to 11 beta-hydroxylase deficiency|Congenital adrenal hyperplasia due to 11β-hydroxylase deficiency]]
{{Familytree/end}}
 
====Biochemistry====
====Biochemistry====
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Revision as of 16:56, 21 January 2016

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

Overview

Congenital Adrenal Hyperplasia

Production of DHEA from Cholesterol. (Cortisol is a glucocorticoid.)

Classification

 
 
 
 
 
 
 
 
 
 
 
 
 
Congenital Adrenal Hyperplasia
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
Lipoid congenital adrenal hyperplasia
 
 
Congenital adrenal hyperplasia due to 21-hydroxylase deficiency
 
 
 
 
 
 
 
Congenital adrenal hyperplasia due to 17 alpha-hydroxylase deficiency
 
 
Congenital adrenal hyperplasia due to 3 beta-hydroxysteroid dehydrogenase deficiency
 
Congenital adrenal hyperplasia due to 11 beta-hydroxysteroid dehydrogenase deficiency
 
 
 
 
 
 
 

Biochemistry

Common medical term OMIM no. Enzyme(s) Gene location Substrate(s) Product(s)
21-hydroxylase CAH Online Mendelian Inheritance in Man (OMIM) 201910 P450c21 6p21.3 17OH-progesterone→
progesterone
11-deoxycortisol
DOC
lipoid CAH
(20,22-desmolase)
Online Mendelian Inheritance in Man (OMIM) 201710 StAR
P450scc
8p11.2
15q23-q24
transport of cholesterol
cholesterol
into mitochondria
pregnenolone
17α-hydroxylase CAH Online Mendelian Inheritance in Man (OMIM) 202110 P450c17 10q24.3 pregnenolone
progesterone
17OH-pregnenolone→
17OH-pregnenolone
17OH-progesterone
DHEA
3β-HSD CAH Online Mendelian Inheritance in Man (OMIM) 201810 3βHSD II 1p13 pregnenolone
17OH-pregnenolone→
DHEA
progesterone
17OH-progesterone
androstenedione
11β-hydroxylase CAH Online Mendelian Inheritance in Man (OMIM) 202010 P450c11β 8q21-22 11-deoxycortisol→
DOC→
cortisol
corticosterone

Reference