21-hydroxylase deficiency: Difference between revisions
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'''For patient information click [[{{PAGENAME}} (patient information)|here]]''' | '''For patient information click [[{{PAGENAME}} (patient information)|here]]''' | ||
{{21-hydroxylase deficiency}} | {{21-hydroxylase deficiency}} | ||
{{CMG}} {{MJ}} | {{CMG}}; {{AE}} {{MJ}} {{AAM}} | ||
{{SK}} Congenital adrenal hyperplasia due to | {{SK}} Congenital adrenal hyperplasia due to 21-hydroxylase deficiency; 21-hydroxylase deficient congenital adrenal hyperplasia; CAH1; CYP21A deficiency; Congenital adrenal hyperplasia 1 | ||
==[[21-hydroxylase deficiency overview|Overview]]== | ==[[21-hydroxylase deficiency overview|Overview]]== | ||
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==[[21-hydroxylase deficiency causes|Causes]]== | ==[[21-hydroxylase deficiency causes|Causes]]== | ||
==[[21-hydroxylase deficiency differential diagnosis|Differentiating | ==[[21-hydroxylase deficiency differential diagnosis|Differentiating 21-hydroxylase deficiency from other Diseases]]== | ||
==[[21-hydroxylase deficiency epidemiology and demographics|Epidemiology and Demographics]]== | ==[[21-hydroxylase deficiency epidemiology and demographics|Epidemiology and Demographics]]== | ||
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[[Category:Endocrinology]] | [[Category:Endocrinology]] | ||
[[Category:Genetic disorders]] | [[Category:Genetic disorders]] | ||
[[Category:Intersexuality]] | |||
[[Category:Medicine]] | |||
[[Category:Up-To-Date]] | |||
{{WikiDoc Help Menu}} | {{WikiDoc Help Menu}} | ||
{{WikiDoc Sources}} | {{WikiDoc Sources}} |
Latest revision as of 21:08, 25 July 2020
For patient information click here
21-hydroxylase deficiency Microchapters |
Differentiating 21-Hydroxylase Deficiency from other Diseases |
Diagnosis |
Treatment |
Case Studies |
21-hydroxylase deficiency On the Web |
American Roentgen Ray Society Images of 21-hydroxylase deficiency |
Risk calculators and risk factors for 21-hydroxylase deficiency |
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Mehrian Jafarizade, M.D [2] Ahmad Al Maradni, M.D. [3]
Synonyms and keywords: Congenital adrenal hyperplasia due to 21-hydroxylase deficiency; 21-hydroxylase deficient congenital adrenal hyperplasia; CAH1; CYP21A deficiency; Congenital adrenal hyperplasia 1
Overview
Historical Perspective
Classification
Pathophysiology
Causes
Differentiating 21-hydroxylase deficiency from other Diseases
Epidemiology and Demographics
Risk Factors
Screening
Natural History, Complications and Prognosis
Diagnosis
History and Symptoms | Physical Examination | Laboratory Findings | Electrocardiogram | CT | MRI | Ultrasound | Other Imaging Findings | Other Diagnostic Studies
Treatment
Medical Therapy | Surgery | Primary Prevention | Secondary Prevention | Cost-Effectiveness of Therapy | Future or Investigational Therapies
Case Studies
Related Chapters