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What is Maroteaux-Fonfria syndrome?

What is Maroteaux-Fonfria syndrome?

  • Maroteaux-Fonfria syndrome: A rare congenital disorder characterized by extra little fingers and extra big toes as well as the normal features associated with Apert syndrome.

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

Maroteaux-Fonfria syndrome: Introduction

Types of Maroteaux-Fonfria syndrome:

Broader types of Maroteaux-Fonfria syndrome:

What causes Maroteaux-Fonfria syndrome?

Causes of Maroteaux-Fonfria syndrome: see causes of Maroteaux-Fonfria syndrome

What are the symptoms of Maroteaux-Fonfria syndrome?

Symptoms of Maroteaux-Fonfria syndrome: see symptoms of Maroteaux-Fonfria syndrome

Maroteaux-Fonfria syndrome: Testing

Misdiagnosis: see misdiagnosis and Maroteaux-Fonfria syndrome.

How is it treated?

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

Name and Aliases of Maroteaux-Fonfria syndrome

Main name of condition: Maroteaux-Fonfria syndrome

Other names or spellings for Maroteaux-Fonfria syndrome:

Apparent Apert syndrome with polydactyly, Apert syndrome with polydactyly of hands and feet

Apert syndrome with polydactyly of hands and feet, Apparent Apert syndrome with polydactyly
Source - Office of Rare Diseases (ORD) of the National Institutes of Health (NIH)


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