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

• Sensitivity to light
• Rapid involuntary eye movements
• Altered color vision
• Teeth discoloration
• Abnormal teeth shape

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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