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What is Faciothoracogenital syndrome?

What is Faciothoracogenital syndrome?

  • Faciothoracogenital syndrome: A rare syndrome characterized by facial, chest and genital abnormalities.

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

Faciothoracogenital syndrome: Introduction

Types of Faciothoracogenital syndrome:

Broader types of Faciothoracogenital syndrome:

What causes Faciothoracogenital syndrome?

Causes of Faciothoracogenital syndrome: see causes of Faciothoracogenital syndrome

What are the symptoms of Faciothoracogenital syndrome?

Symptoms of Faciothoracogenital syndrome: see symptoms of Faciothoracogenital syndrome

Faciothoracogenital syndrome: Testing

Diagnostic testing: see tests for Faciothoracogenital syndrome.

Misdiagnosis: see misdiagnosis and Faciothoracogenital syndrome.

How is it treated?

Doctors and Medical Specialists for Faciothoracogenital syndrome: Neonatologist ; see also doctors and medical specialists for Faciothoracogenital syndrome.
Treatments for Faciothoracogenital syndrome: see treatments for Faciothoracogenital syndrome

Name and Aliases of Faciothoracogenital syndrome

Main name of condition: Faciothoracogenital syndrome

Other names or spellings for Faciothoracogenital syndrome:

Congenital anomalies, involving mainly the face, thorax, and genitalia

Congenital anomalies, involving mainly the face, thorax, and genitalia
Source - Office of Rare Diseases (ORD) of the National Institutes of Health (NIH)

 

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