Living with Distal trisomy 19q
A rare chromosome condition with low birth weight, delays in development, short height, and distinct facial features.
Understanding Distal trisomy 19q
People with this condition often have low birth weight, delays in development, intellectual disability, and short height. Facial features can include a small head, a small lower jaw, and a short neck with extra skin folds. Low muscle tone, bone differences in the fingers, seizures, and differences in the heart, urinary and genital, and digestive systems may also occur. Signs show up in the newborn and infant years.
Signs & symptoms
GARD doesn't list specific symptoms for this condition separately, but the summary describes these features:
- Low birth weight
- Delays in development
- Intellectual disability
- Short height
- Low muscle tone (hypotonia)
- Seizures
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
GARD says changes in a person's genes cause this condition. The summary describes it as an extra copy of part of the long arm of chromosome 19.
Also known as: distal duplication 19q; distal trisomy 19q syndrome; distal trisomy type 19q; telomeric duplication 19q; trisomy 19qter
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 Distal trisomy 19q.
Explore research for Distal trisomy 19q
Explore actively recruiting Distal trisomy 19q studies with HealthSpark.
Find actively recruiting studies for Distal trisomy 19q 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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