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Cone rod dystrophy - amelogenesis imperfecta



Introduction: Cone rod dystrophy - amelogenesis imperfecta

Cone rod dystrophy - amelogenesis imperfecta: A rare genetic disorder characterized by degeneration of parts of the eye that absorb light (cone rod dystrophy) as well as teeth abnormalities. More detailed information about the symptoms, causes, and treatments of Cone rod dystrophy - amelogenesis imperfecta is available below.

Symptoms of Cone rod dystrophy - amelogenesis imperfecta

Read more about symptoms of Cone rod dystrophy - amelogenesis imperfecta

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Definitions of Cone rod dystrophy - amelogenesis imperfecta:

Ophanet, a consortium of European partners, currently defines a condition rare when it affects 1 person per 2,000. They list Cone rod dystrophy - amelogenesis imperfecta as a "rare disease".
Source - Orphanet


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