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| '''For the WikiDoc page for this topic, click [[Congenital adrenal hyperplasia|here]]'''
| | #REDIRECT [[Congenital adrenal hyperplasia due to 21-hydroxylase deficiency (patient information)]] |
| {{SI}}
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| {{CMG}}; '''Associate Editor(s)-In-Chief:''' Jinhui Wu, M.D.
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| ==Overview==
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| Congenital adrenal hyperplasia refers to genetic disorders of the [[adrenal gland]]s. It includes a group of autosomal recessive conditions resulting from biochemical paths of the [[steroidogenesis]] of [[cortisol]] from [[cholesterol]] by the [[adrenal gland]]s. These diseases are [[21-hydroxylase deficiency]], 17α-hydroxylase deficiency, 11β-hydroxylase deficiency, 3β-hydroxysteroid dehydrogenase deficiency, etc. Among them, almost 95% of cases of congenital adrenal hyperplasia are due to 21-hydroxylase deficiency. Gene [[mutation]]s are the cause of these diseases. Most of these disorders can interfere with normal growth and development in children and adults.
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| ==See also==
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| :*[[Congenital adrenal hyperplasia due to 21-hydroxylase deficiency (patient information)]]
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| ==Copyleft Sources==
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| http://www.mayoclinic.com/print/congenital-adrenal-hyperplasia/DS00915/METHOD=print&DSECTION=all
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| http://www.nlm.nih.gov/medlineplus/ency/article/000411.htm
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| http://www.nichd.nih.gov/health/topics/Congenital_Adrenal_Hyperplasia.cfm
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| [[Category:Disease state]]
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| [[Category:Medicine]]
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| [[Category:Endocrinology]]
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| [[Category:Oncology]]
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| [[Category:Growth disorders]]
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| [[Category:Endocrinology patient information]]
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| [[Category:Oncology patient information]]
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| [[Category:Autosomal recessive disorders]]
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| [[Category:Intersexuality]]
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| [[Category:Genetics]]
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| [[Category:Patient information]]
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| [[Category:Genetic disorders patient information]]
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| [[Category:Mature chapter]]
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| {{WH}}
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| {{WS}}
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