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 21-hydroxylase deficiency; 21-hydroxylase deficiency; 21-hydroxylase deficient congenital adrenal hyperplasia; CAH1; CYP21A deficiency; Congenital adrenal hyperplasia 1
{{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 Congenital Adrenal Hyperplasia due to 21-Hydroxylase Deficiency from other Diseases]]==
==[[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:Genetic disorders]]
[[Category:Genetic disorders]]
[[Category:Intersexuality]]
[[Category:Medicine]]
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[[Category:Intersexuality]]
[[Category:Mature chapter]]




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Latest revision as of 21:08, 25 July 2020


For patient information click here

Congenital adrenal hyperplasia main page

21-hydroxylase deficiency Microchapters

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Overview

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Epidemiology and Demographics

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Case #1

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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

Case#1

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