Living with Dacryocystitis-osteopoikilosis syndrome
An extremely rare inherited condition affecting the tear ducts and bones.
Understanding Dacryocystitis-osteopoikilosis syndrome
It has been reported in only a few people. It causes infection of the tear sac (dacryocystitis) due to narrowing of the tear canal. It also causes small, round, dense spots in the bones (osteopoikilosis) that show up on X-rays.
Signs & symptoms
GARD doesn't list specific symptoms for this condition yet. Its summary describes these features:
- Tear sac infection (dacryocystitis)
- Narrowed tear canal
- Small, dense round spots in bones seen on X-ray
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
Your doctor may refer you to a specialist who knows rare conditions.
- 3Ask which tests can help
Your care team will decide which exams and tests can confirm the diagnosis.
Care & treatment
- Care team
- A doctor familiar with rare conditions, plus specialists as needed
- 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 doesn't name a gene. It lists autosomal dominant inheritance, so a changed copy of a gene from one parent can be enough.
Also known as: dacryocystitis and osteopoikilosis syndrome; gunal seber basaran syndrome; gunal-seber-basaran 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 Dacryocystitis-osteopoikilosis syndrome.
Explore research for Dacryocystitis-osteopoikilosis syndrome
Explore actively recruiting Dacryocystitis-osteopoikilosis syndrome studies with HealthSpark.
Find actively recruiting studies for Dacryocystitis-osteopoikilosis 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
Powered by HealthSpark, our AI chat helper
I can help you find recruiting Dacryocystitis-osteopoikilosis syndrome studies. Enter a ZIP code, address or city below and I'll look within 50 miles.
Powered by HealthSpark, our AI chat helper · Study information from ClinicalTrials.gov · Eligibility is confirmed by the study team.
Get Signals for Dacryocystitis-osteopoikilosis syndrome
Stay in the loop with community stories and updates from medical researchers.
Create a living journal that talks back
HealthStory evolves private journaling with a living AI journal that talks back and asks thoughtful questions, helping you capture your Dacryocystitis-osteopoikilosis syndrome experiences more deeply and prepare for better conversations with your doctors and care team.
Your journal is private. Sharing your story publicly is a separate choice, made with Share your story above.