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What is Amelogenesis Imperfecta hypomaturation type?

What is Amelogenesis Imperfecta hypomaturation type?

  • Amelogenesis Imperfecta hypomaturation type: Amelogenesis imperfecta is an inherited tooth development disorder characterized by tooth enamel defects. The hypomaturation type involves an abnormality during the maturation stage of enamel formation which causes the enamel to become porous and opaque.

Amelogenesis Imperfecta 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 hypomaturation type, or a subtype of Amelogenesis Imperfecta hypomaturation type, affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)

Amelogenesis Imperfecta hypomaturation type: Introduction

Types of Amelogenesis Imperfecta hypomaturation type:

Broader types of Amelogenesis Imperfecta hypomaturation type:

What causes Amelogenesis Imperfecta hypomaturation type?

Causes of Amelogenesis Imperfecta hypomaturation type: see causes of Amelogenesis Imperfecta hypomaturation type

What are the symptoms of Amelogenesis Imperfecta hypomaturation type?

Symptoms of Amelogenesis Imperfecta hypomaturation type: see symptoms of Amelogenesis Imperfecta hypomaturation type

How is it treated?

Doctors and Medical Specialists for Amelogenesis Imperfecta hypomaturation type: Medical Geneticist ; see also doctors and medical specialists for Amelogenesis Imperfecta hypomaturation type.
Treatments for Amelogenesis Imperfecta hypomaturation type: see treatments for Amelogenesis Imperfecta hypomaturation type

Name and Aliases of Amelogenesis Imperfecta hypomaturation type

Main name of condition: Amelogenesis Imperfecta hypomaturation type

Other names or spellings for Amelogenesis Imperfecta hypomaturation type:

AIH, amelogeneses imperfecta, type II

AIH
Source - Office of Rare Diseases (ORD) of the National Institutes of Health (NIH)

 

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