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What is Multiple fibrofolliculoma familial?

What is Multiple fibrofolliculoma familial?

  • Multiple fibrofolliculoma familial: A rare familial genetic disorder characterized by the development of numerous benign hair follicle tumors.

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

Multiple fibrofolliculoma familial: Introduction

Types of Multiple fibrofolliculoma familial:

Broader types of Multiple fibrofolliculoma familial:

What causes Multiple fibrofolliculoma familial?

Causes of Multiple fibrofolliculoma familial: see causes of Multiple fibrofolliculoma familial

What are the symptoms of Multiple fibrofolliculoma familial?

Symptoms of Multiple fibrofolliculoma familial: see symptoms of Multiple fibrofolliculoma familial

Multiple fibrofolliculoma familial: Testing

Diagnostic testing: see tests for Multiple fibrofolliculoma familial.

Misdiagnosis: see misdiagnosis and Multiple fibrofolliculoma familial.

How is it treated?

Doctors and Medical Specialists for Multiple fibrofolliculoma familial: Medical Geneticist ; see also doctors and medical specialists for Multiple fibrofolliculoma familial.
Treatments for Multiple fibrofolliculoma familial: see treatments for Multiple fibrofolliculoma familial

Name of Multiple fibrofolliculoma familial

Main name of condition: Multiple fibrofolliculoma familial

 

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