Living with CODAS syndrome
A rare syndrome with brain, eye, tooth, ear, and bone differences.
Understanding CODAS syndrome
GARD lists onset in the newborn period and infancy. It can include cataracts, tooth enamel differences, spine and hip bone differences, and crumpled ears.
Signs & symptoms
Symptoms vary from person to person. GARD lists these among the most common:
- Cataracts
- Differences in tooth shape and enamel
- Differences in spine bones
- Differences in the hip bones
- Crumpled ears
- Differences at the ends of long bones
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, brain and nervous system specialists, eye disease specialists and genetic specialists.
- 3Consider genetic testing
Changes in LONP1 are linked to this condition. Genetic testing and counseling can help confirm a diagnosis and explain what it means for your family.
Care & treatment
- Care team
- Bone and joint specialists (orthopedists or orthopedic surgeons); Brain and nervous system specialists (neurologists); Eye disease specialists (ophthalmologists); 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
GARD says changes in the LONP1 gene cause this condition. It is autosomal recessive, so a child inherits a changed copy of the gene from each parent.
Also known as: cerebral, ocular, dental, auricular, and skeletal anomalies syndrome; cerebro-oculo-dento-auriculo-skeletal syndrome; cerebrooculodentoauriculoskeletal syndrome; codas (cerebro-oculo-dento-auriculo-skeletal) syndrome
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 CODAS syndrome.
Explore research for CODAS syndrome
Explore actively recruiting CODAS syndrome studies with HealthSpark.
Find actively recruiting studies for CODAS syndrome with HealthSpark. Share your city to explore research near you.
- Recruiting studies from ClinicalTrials.gov
- Share your city to look for research near you
- 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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