Living with Ring chromosome 15
A rare chromosome change that affects growth, learning, and speech, with short height and low muscle tone.
Understanding Ring chromosome 15
People often have slow growth before and after birth, resulting in short stature, along with intellectual disability, low muscle tone, and facial and limb differences. Other features can include heart defects, kidney problems, hip dislocation, and café-au-lait spots. GARD says it usually arises by chance early in development, but rarely is passed through a family.
Signs & symptoms
Symptoms vary from person to person. GARD lists these among the most common:
- Short stature
- Slow growth before birth
- Global developmental delay
- Intellectual disability
- Feeding difficulties in infancy
- Small head size and triangular face
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.
- 3Ask which tests can help
Your care team will decide which exams and tests can confirm the diagnosis.
Care & treatment
- Care team
- 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 Chromosome Disorder Outreach
- 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
It happens when chromosome 15 forms a ring and genetic material is lost from its long arm. It usually arises by chance, and in rare cases is passed down from a parent.
Also known as: chromosome 15 ring; ring 15; ring chromosome 15 syndrome; ring chromosome type 15
Patient organizations
- Chromosome Disorder OutreachChromosome disorders · United States
Broader rare-disease groups
- 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 Ring chromosome 15.
Explore research for Ring chromosome 15
Explore actively recruiting Ring chromosome 15 studies with HealthSpark.
Find actively recruiting studies for Ring chromosome 15 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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