Living with Dentinogenesis imperfecta type 3
A rare, severe form of dentinogenesis imperfecta with discolored, see-through, weak teeth.
Understanding Dentinogenesis imperfecta type 3
Teeth are generally discolored, most often blue-gray or yellow-brown, and translucent. They are weaker than normal and wear down, break, and may be lost. Both baby and permanent teeth are affected. GARD lists onset in childhood.
Signs & symptoms
GARD doesn't list a symptom list. Based on its summary, features include:
- Blue-gray or yellow-brown teeth
- See-through (translucent) teeth
- Weak teeth that wear and break easily
Not everyone has every symptom. GARD's list comes from the Human Phenotype Ontology.
Diagnosis
- 1Talk with your doctor
Share the symptoms you've noticed, when they started and your family health history. Notes and photos can help.
- 2See a specialist
Specialists who may be involved include genetic specialists and gum, teeth and mouth specialists.
- 3Consider genetic testing
Changes in DSPP are linked to this condition. Genetic testing and counseling can help confirm a diagnosis and explain what it means for your family.
- 4Connect with expert centers
Osteogenesis Imperfecta Foundation may keep lists of experts for this condition.
Care & treatment
- Care team
- Genetic specialists (geneticists); Gum, teeth and mouth specialists (odontologists)
- Expert care
- Expert lists: Osteogenesis Imperfecta Foundation
- Treatment
- GARD doesn't list specific treatments for this condition. Your care team will tailor care to your symptoms.
- Research
- Clinical trials and observational studies may be options. See the research section below.
General information, not medical advice. Your care team makes the decisions.
Everyday life
Living with a rare condition is easier with support.
- Connect with Osteogenesis Imperfecta Foundation
- Keep notes on symptoms, changes and questions for appointments
- Ask about patient registries that help research
- Look into financial aid and travel resources for care visits
Quick facts
Changes in the DSPP gene cause this condition. It is autosomal dominant, so a changed copy of the gene from one parent can be enough.
Also known as: brandywine type dentinogenesis imperfecta; brandywine type of dentinogenesis imperfecta; dentinogenesis imperfecta - shield's type iii; dentinogenesis imperfecta shields type 3; dentinogenesis imperfecta type iii; dentinogenesis imperfecta, shields type 3
Patient organizations
- Osteogenesis Imperfecta FoundationDentinogenesis imperfecta type 3 · United States
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Perspectives from people navigating life with Dentinogenesis imperfecta type 3.
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- Recruiting studies from ClinicalTrials.gov
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- Eligibility is confirmed by the study team
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Powered by HealthSpark, our AI chat helper · Study information from ClinicalTrials.gov · Eligibility is confirmed by the study team.
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