Osteogenesis Imperfecta

Overview

COLLAGEN DISEASES characterized by brittle, osteoporotic, and easily fractured bones. It may also present with blue sclerae, loose joints, and imperfect dentin formation. Most types are autosomal dominant and are associated with mutations in COLLAGEN TYPE I.

This information is general and should not be treated as medical advice. Always speak directly with a qualified healthcare professional before making decisions about treatment, diagnosis, procedures, medicines or care.

Quick facts about Osteogenesis Imperfecta

Topic type

Condition

Category

Dermatology

MeSH classification

C05.116.099.708.685|C16.320.737|C17.300.200.540

Preparing for an appointment about Osteogenesis Imperfecta

If you are speaking with a healthcare professional about Osteogenesis Imperfecta, it can help to prepare a few details in advance.

• Write down your symptoms and when they started.
• Bring details of any medicines, supplements or previous treatments.
• Ask what tests or assessments may be needed.
• Ask what treatment or management options may be suitable.
• Ask when you should seek urgent medical help or follow-up care.

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