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Living with Intracranial berry aneurysm

A condition in which a weak spot in a brain artery bulges like a sac; it can run in families.

Understanding Intracranial berry aneurysm

Intracranial berry aneurysm is a rare genetic condition with a sac-like bulge in an artery of the brain, from a weak artery wall.

It is suspected as familial when two or more close relatives are affected. An aneurysm may cause no symptoms for life, or it can rupture and cause bleeding around the brain (subarachnoid hemorrhage). People with the familial form are more likely to have more than one aneurysm and a higher chance of rupture.

Signs & symptoms

Symptoms vary from person to person. GARD lists these among the most common:

  • Bulging brain artery (berry aneurysm)
  • High blood pressure
  • Mini stroke (transient ischemic attack)
  • Narrowed, hardened arteries
  • Bleeding around the brain (subarachnoid hemorrhage)
  • Differences in the circle of Willis

Not everyone has every symptom. GARD's list comes from the Human Phenotype Ontology.

Diagnosis

  1. Talk with your doctor

    Share the symptoms you've noticed, when they started and your family health history. Notes and photos can help.

  2. See a specialist

    Specialists who may be involved include brain and nervous system specialists and genetic specialists.

  3. Ask which tests can help

    Your care team will decide which exams and tests can confirm the diagnosis.

Care & treatment

Care team
Brain and nervous system specialists (neurologists); 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 The Aneurysm and AVM Foundation
  • 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
Bring these questions to your next doctor visit
Should my relatives be screened for aneurysms?
How will you monitor the size of my aneurysm?
Which symptoms need emergency care?

Quick facts

Symptoms usually startany time in life
InheritanceAutosomal Dominant, Autosomal Recessive

GARD lists autosomal dominant and autosomal recessive inheritance. It doesn't name a gene.

GeneticNeurological

Also known as: aneurysm, intracranial berry; familial aneurysmal subarachnoid haemorrhage; familial aneurysmal subarachnoid hemorrhage; familial berry aneurysm; familial cerebral saccular aneurysm; familial intracranial saccular aneurysm

Patient organizations

Source: NIH GARD · Intracranial berry aneurysmGARD ID 17161 · GARD page updated September 2026 · Plain-language summary by Know Rare; editorial review pending. General information, not medical advice.

You are more than your diagnosis

Perspectives from people navigating life with Intracranial berry aneurysm.

Explore the Intracranial berry aneurysm blog

Explore research for Intracranial berry aneurysm

Explore actively recruiting Intracranial berry aneurysm studies with HealthSpark.

HealthSpark

Find actively recruiting studies for Intracranial berry aneurysm with HealthSpark. Share your city to explore research near you.

  • 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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