
Living with Multiple gastrointestinal atresias
A rare condition in which parts of the intestine are blocked from before birth, causing problems in newborns.
Understanding Multiple gastrointestinal atresias
In this condition, there are many blocked segments (atresias) in the small bowel or large bowel. This causes signs of a blockage in newborns, such as vomiting, a swollen belly, and being unable to pass the first stool (meconium). It can sometimes be seen during pregnancy.
Signs & symptoms
Symptoms vary from person to person. GARD lists these among the most common:
- Blocked sections of the intestine (atresia)
- Narrowing of the first part of the small bowel
- Extra amniotic fluid in pregnancy (polyhydramnios)
- Vomiting in newborns
- Swollen belly
- Unable to pass the first stool (meconium)
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 digestive system 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
- Digestive system specialists (gastroenterologists); 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 genes cause this condition. A child inherits a changed copy of a gene from each parent (autosomal recessive).
Also known as: familial intestinal polyatresia syndrome; isolated multiple intestinal atresia; multiple intestinal atresia
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 Multiple gastrointestinal atresias.
Explore research for Multiple gastrointestinal atresias
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- Recruiting studies from ClinicalTrials.gov
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- 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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