17 alpha-hydroxylase deficiency screening: Difference between revisions

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==Overview==
==Overview==
There is insufficient evidence to recommend routine screening for 11β-hydroxylase deficiency.  
There is insufficient evidence to recommend routine screening for 17 alpha-hydroxylase deficiency.  
==Screening==
==Screening==
There is insufficient evidence to recommend routine screening for 11β-hydroxylase deficiency.  
There is insufficient evidence to recommend routine screening for 17 alpha-hydroxylase deficiency.  
==References==
==References==
{{Reflist|2}}
{{Reflist|2}}

Latest revision as of 18:04, 7 August 2017

Congenital adrenal hyperplasia main page

17 alpha-hydroxylase deficiency Microchapters

Home

Patient Information

Overview

Historical Perspective

Classification

Pathophysiology

Causes

Differentiating 17 alpha-hydroxylase deficiency from other Diseases

Epidemiology and Demographics

Risk Factors

Screening

Natural History, Complications and Prognosis

Diagnosis

History and Symptoms

Physical Examination

Laboratory Findings

CT

MRI

Ultrasound

Other Imaging Findings

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Treatment

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Case #1

17 alpha-hydroxylase deficiency screening On the Web

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Directions to Hospitals Treating Congenital adrenal hyperplasia due to 17 alpha-hydroxylase deficiency

Risk calculators and risk factors for 17 alpha-hydroxylase deficiency screening

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

Overview

There is insufficient evidence to recommend routine screening for 17 alpha-hydroxylase deficiency.

Screening

There is insufficient evidence to recommend routine screening for 17 alpha-hydroxylase deficiency.

References