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Lipoid congenital adrenal hyperplasia

Lipoid congenital adrenal hyperplasia: Introduction

Lipoid congenital adrenal hyperplasia: A rare form of congenital adrenal hyperplasia where the early phase of adrenal cortisol production is defective which causes mineralocorticoid deficiency. Male pseudohermaphroditism is the main characteristic of this disorder. More detailed information about the symptoms, causes, and treatments of Lipoid congenital adrenal hyperplasia is available below.

Symptoms of Lipoid congenital adrenal hyperplasia

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Lipoid congenital adrenal hyperplasia: Related Patient Stories

Lipoid congenital adrenal hyperplasia: Complications

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Causes of Lipoid congenital adrenal hyperplasia

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Disease Topics Related To Lipoid congenital adrenal hyperplasia

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Less Common Symptoms of Lipoid congenital adrenal hyperplasia

Lipoid congenital adrenal hyperplasia: Undiagnosed Conditions

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Misdiagnosis and Lipoid congenital adrenal hyperplasia

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Lipoid congenital adrenal hyperplasia: Research Doctors & Specialists

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Hospitals & Clinics: Lipoid congenital adrenal hyperplasia

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Lipoid congenital adrenal hyperplasia: Rare Types

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Lipoid congenital adrenal hyperplasia: Animations

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Lipoid congenital adrenal hyperplasia: Broader Related Topics

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Definitions of Lipoid congenital adrenal hyperplasia:

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

 

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