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Faciothoracogenital syndrome

Faciothoracogenital syndrome: Introduction

Faciothoracogenital syndrome: A rare syndrome characterized by facial, chest and genital abnormalities. More detailed information about the symptoms, causes, and treatments of Faciothoracogenital syndrome is available below.

Symptoms of Faciothoracogenital syndrome

Home Diagnostic Testing

Home medical testing related to Faciothoracogenital syndrome:

Wrongly Diagnosed with Faciothoracogenital syndrome?

Faciothoracogenital syndrome: Related Patient Stories

Causes of Faciothoracogenital syndrome

Read more about causes of Faciothoracogenital syndrome.

Faciothoracogenital syndrome: Undiagnosed Conditions

Commonly undiagnosed diseases in related medical categories:

Hospitals & Clinics: Faciothoracogenital syndrome

Research quality ratings and patient safety measures for medical facilities in specialties related to Faciothoracogenital syndrome:

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

Statistics for Faciothoracogenital syndrome

Faciothoracogenital syndrome: Broader Related Topics

User Interactive Forums

Read about other experiences, ask a question about Faciothoracogenital syndrome, or answer someone else's question, on our message boards:

Definitions of Faciothoracogenital syndrome:

Faciothoracogenital syndrome is listed as a "rare disease" by the Office of Rare Diseases (ORD) of the National Institutes of Health (NIH). This means that Faciothoracogenital syndrome, or a subtype of Faciothoracogenital syndrome, 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 Faciothoracogenital syndrome as a "rare disease".
Source - Orphanet

 

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