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Adrenal adenoma, familial

Adrenal adenoma, familial: Introduction

Adrenal adenoma, familial: A benign tumor that develops in the adrenal gland and tends to run in families. The tumor may be nonfunctioning (does not produce hormones) or functioning in which case excessive levels of hormones can cause a variety of symptoms depending on which hormone is involved. Adrenal hormones made in the cortex (outer part of the gland) are aldosterone, corticosteroids and androgenic steroids . Adrenalin and noradrenalin are the hormones made in the medulla (central part of the adrenal gland). More detailed information about the symptoms, causes, and treatments of Adrenal adenoma, familial is available below.

Symptoms of Adrenal adenoma, familial

Home Diagnostic Testing

Home medical testing related to Adrenal adenoma, familial:

Wrongly Diagnosed with Adrenal adenoma, familial?

Adrenal adenoma, familial: Related Patient Stories

Causes of Adrenal adenoma, familial

Read more about causes of Adrenal adenoma, familial.

Disease Topics Related To Adrenal adenoma, familial

Research the causes of these diseases that are similar to, or related to, Adrenal adenoma, familial:

Adrenal adenoma, familial: Undiagnosed Conditions

Commonly undiagnosed diseases in related medical categories:

Misdiagnosis and Adrenal adenoma, familial

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Adrenal adenoma, familial: Research Doctors & Specialists

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Hospitals & Clinics: Adrenal adenoma, familial

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Choosing the Best Hospital: More general information, not necessarily in relation to Adrenal adenoma, familial, on hospital performance and surgical care quality:

Adrenal adenoma, familial: Rare Types

Rare types of diseases and disorders in related medical categories:

Statistics for Adrenal adenoma, familial

Adrenal adenoma, familial: Broader Related Topics

User Interactive Forums

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Definitions of Adrenal adenoma, familial:

Ophanet, a consortium of European partners, currently defines a condition rare when it affects 1 person per 2,000. They list Adrenal adenoma, familial as a "rare disease".
Source - Orphanet


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