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Adrenal hyperplasia, congenital type 3

Adrenal hyperplasia, congenital type 3: Introduction

Adrenal hyperplasia, congenital type 3: A group of disorders that occur when a deficiency of 21-hydroxylase impairs the normal process of making adrenal corticosteroids. The severity of the condition is variable depending on the degree of deficiency. More detailed information about the symptoms, causes, and treatments of Adrenal hyperplasia, congenital type 3 is available below.

Symptoms of Adrenal hyperplasia, congenital type 3

Home Diagnostic Testing

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Wrongly Diagnosed with Adrenal hyperplasia, congenital type 3?

Adrenal hyperplasia, congenital type 3: Related Patient Stories

Adrenal hyperplasia, congenital type 3: Complications

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Causes of Adrenal hyperplasia, congenital type 3

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Adrenal hyperplasia, congenital type 3: Undiagnosed Conditions

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Misdiagnosis and Adrenal hyperplasia, congenital type 3

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Adrenal hyperplasia, congenital type 3: Research Doctors & Specialists

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Definitions of Adrenal hyperplasia, congenital type 3:

Adrenal hyperplasia, congenital type 3 is listed as a "rare disease" by the Office of Rare Diseases (ORD) of the National Institutes of Health (NIH). This means that Adrenal hyperplasia, congenital type 3, or a subtype of Adrenal hyperplasia, congenital type 3, affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)

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More information about Adrenal hyperplasia, congenital type 3

  1. Adrenal hyperplasia, congenital type 3: Introduction
  2. Symptoms
  3. Causes
  4. Treatments
  5. Misdiagnosis
  6. Home Testing
  7. Complications
 

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