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Amelogenesis imperfecta pigmented hypomaturation type

Amelogenesis imperfecta pigmented hypomaturation type: Introduction

Amelogenesis imperfecta pigmented hypomaturation type: Amelogenesis imperfecta is an inherited tooth development disorder characterized by tooth enamel defects. The pigmented hypomaturation type is characterized by fragile tooth enamel which tends to be soft and rough and is usually a creamy to yellow/brown color. More detailed information about the symptoms, causes, and treatments of Amelogenesis imperfecta pigmented hypomaturation type is available below.

Symptoms of Amelogenesis imperfecta pigmented hypomaturation type

Wrongly Diagnosed with Amelogenesis imperfecta pigmented hypomaturation type?

Amelogenesis imperfecta pigmented hypomaturation type: Related Patient Stories

Causes of Amelogenesis imperfecta pigmented hypomaturation type

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Misdiagnosis and Amelogenesis imperfecta pigmented hypomaturation type

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Amelogenesis imperfecta pigmented hypomaturation type: Research Doctors & Specialists

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Definitions of Amelogenesis imperfecta pigmented hypomaturation type:

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

 

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