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Leiomyomatosis familial

Leiomyomatosis familial: Introduction

Leiomyomatosis familial: A rare syndrome characterized by the development of a number of benign skin tumors that develops from smooth muscle tissue. In familial cases, the condition occurs in several members of a family. Tumors may also occur in other parts of the body. More detailed information about the symptoms, causes, and treatments of Leiomyomatosis familial is available below.

Symptoms of Leiomyomatosis familial

Home Diagnostic Testing

Home medical testing related to Leiomyomatosis familial:

Wrongly Diagnosed with Leiomyomatosis familial?

Causes of Leiomyomatosis familial

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Less Common Symptoms of Leiomyomatosis familial

Leiomyomatosis familial: Undiagnosed Conditions

Commonly undiagnosed diseases in related medical categories:

Misdiagnosis and Leiomyomatosis familial

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Leiomyomatosis familial: Research Doctors & Specialists

Research related physicians and medical specialists:

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Hospitals & Clinics: Leiomyomatosis familial

Research quality ratings and patient safety measures for medical facilities in specialties related to Leiomyomatosis familial:

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

Leiomyomatosis familial: Rare Types

Rare types of diseases and disorders in related medical categories:

Evidence Based Medicine Research for Leiomyomatosis familial

Medical research articles related to Leiomyomatosis familial include:

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Leiomyomatosis familial: Animations

Research about Leiomyomatosis familial

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Statistics for Leiomyomatosis familial

Leiomyomatosis familial: Broader Related Topics

User Interactive Forums

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Definitions of Leiomyomatosis familial:

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

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

Related Leiomyomatosis familial Info

More information about Leiomyomatosis familial

  1. Leiomyomatosis familial: Introduction
  2. Symptoms
  3. Causes
  4. Treatments
  5. Misdiagnosis
  6. Home Testing
  7. Types
 

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