Living with Familial osteodysplasia, Anderson type
A very rare genetic bone condition affecting the face, jaw, teeth, spine and other bones, described in few reports.
Understanding Familial osteodysplasia, Anderson type
Features include a flattened midface, a broad flat nose bridge, a narrow jaw with a pointed chin, teeth that don't line up, and missing teeth. Other bone differences such as curved spine (scoliosis) can occur. High uric acid and high blood pressure have also been reported. There have been no new descriptions in the medical literature since 1982.
Signs & symptoms
Symptoms vary from person to person. GARD lists these among the most common:
- Flat midface and flat nose
- Large lower jaw
- Teeth out of position or not coming in
- Dental cavities
- Increased risk of fractures
- High blood pressure
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 bone and joint specialists and genetic specialists.
- 3Ask which tests can help
Your care team will decide which exams and tests can confirm the diagnosis.
Care & treatment
- Care team
- Bone and joint specialists (orthopedists or orthopedic surgeons); Genetic specialists (geneticists)
- Expert care
- Ask about multidisciplinary care centers for rare conditions
- 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 rare disease patient organizations for support
- 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 genes cause it. GARD doesn't name a gene or describe how it is inherited.
Also known as: familial osteodysplasia anderson type
Patient organizations
Rare-disease groups that can help
- Global GenesRare Diseases · United States
- National Organization for Rare DisordersRare Diseases · United States
- Genetic AllianceRare Diseases · United States
- RARE FoundationRare Diseases · United States
You are more than your diagnosis
Perspectives from people navigating life with Familial osteodysplasia, Anderson type.
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