Glaucoma is a group of eye conditions that can gradually damage the optic nerve and lead to vision loss; often without noticeable symptoms in its early stages. One of the most common questions people ask is whether glaucoma is hereditary. Research shows that genetics do play a role. If you have a parent, sibling, or close relative with glaucoma, your risk of developing the condition is significantly higher. Specific gene mutations such as MYOC, OPTN, and CYP1B1 have been linked to various types of glaucoma, including primary open-angle glaucoma, normal-tension glaucoma, and congenital forms that appear in early childhood.
Family history doesn’t mean you’re guaranteed to develop glaucoma. Other factors, such as age, ethnicity, high eye pressure, diabetes, or long-term steroid use, can also influence risk. Because glaucoma often causes no symptoms until it’s more advanced, early detection through regular comprehensive eye exams is key. These exams allow eye care professionals to monitor eye pressure, examine the optic nerve, and detect subtle vision changes before permanent damage occurs.
Whether you have a known genetic risk or simply want to be proactive about your eye health, regular exams and open conversations with your provider are a great way to protect your vision. Provision Eye Care offers thorough evaluations and guidance for patients with or without a family history of glaucoma.
Glaucoma is a group of eye conditions that damage the optic nerve, often leading to gradual vision loss. Commonly known as the “silent thief of sight,” it can progress unnoticed until peripheral vision begins to diminish. A frequently asked question about glaucoma is whether it’s hereditary; and the answer is yes. Having a family history of glaucoma can significantly increase your risk of developing the condition.
In its early stages, glaucoma often causes no pain or obvious vision changes. This makes it difficult to detect without a comprehensive eye exam. As the condition progresses, peripheral vision may gradually narrow, sometimes going unnoticed until it significantly affects daily life.
Symptoms of early or progressing glaucoma may include:
Blurred or patchy peripheral vision
Increased difficulty seeing in low light
Eye discomfort or redness in rare cases
Halos around lights (more common with angle-closure glaucoma)
Slow loss of side vision
Although many symptoms are subtle or absent at first, glaucoma can lead to permanent vision loss if left untreated. That’s why regular eye exams are crucial, especially for people with elevated risk.
A strong link exists between family history and the likelihood of developing glaucoma. If someone has a first-degree relative with glaucoma, a parent or sibling, their own risk of developing the condition is significantly higher.
Factors that suggest a genetic connection include:
Having a parent or sibling diagnosed with glaucoma
Being part of a family with a history of early-onset vision issues
Multiple relatives with the same type of glaucoma
Some types of glaucoma have stronger hereditary patterns than others. For example, primary open-angle glaucoma (POAG) is the most common form and often runs in families.
Scientific studies have linked several gene mutations to different forms of glaucoma. These mutations can impact how the eye manages fluid drainage or how the optic nerve handles pressure over time.
Common genes linked to glaucoma include:
MYOC (Myocilin): Associated with some cases of POAG
OPTN (Optineurin): Linked to normal-tension glaucoma
CYP1B1: Frequently connected to congenital glaucoma
LOXL1: Associated with exfoliation glaucoma
Mutations in these genes don’t guarantee someone will develop glaucoma. Rather, they indicate a higher chance, especially when paired with other risk factors.
In rare cases, glaucoma can appear early in life. This form, called primary congenital glaucoma, often has a clear genetic cause.
Genetic traits related to congenital glaucoma include:
Autosomal recessive inheritance (both parents must carry the gene)
Mutations in CYP1B1 or LTBP2
Occasional association with developmental syndromes
Children with congenital glaucoma may show signs like cloudy eyes, excessive tearing, or unusual sensitivity to light. Early diagnosis and treatment are essential.
While genetics can play a major role, glaucoma often results from a combination of inherited and environmental influences.
Additional risk factors that may increase your chance of developing glaucoma include:
Age 60 or older
African, Asian, or Hispanic ancestry
High eye pressure (intraocular pressure)
Thin corneas
Past eye injury or surgery
Long-term corticosteroid use
Diabetes, high blood pressure, or poor blood circulation
Even without a family history, having one or more of these factors may raise the likelihood of developing glaucoma. That’s why routine eye exams are essential for long-term eye health.
If glaucoma runs in your family, it’s worth paying closer attention to your vision and scheduling comprehensive eye exams more frequently. Knowing your genetic risk can help you and your eye doctor take proactive steps.
Here’s what you can do if glaucoma runs in your family:
Share your family history with your eye care provider
Begin screening earlier than age 40 if recommended
Track changes in peripheral vision over time
Monitor eye pressure and optic nerve health regularly
Some eye doctors may recommend genetic testing in cases involving early-onset glaucoma or strong family patterns. However, testing is just one part of the picture; routine eye exams remain the most practical and reliable way to detect changes early.
Glaucoma can’t be prevented outright, but early detection and consistent monitoring can help reduce the risk of vision loss. The goal is to catch the condition before it affects quality of life.
Preventive steps for those with or without a genetic risk include:
Attending routine comprehensive eye exams
Maintaining healthy blood pressure and blood sugar levels
Using prescribed eye drops or medications as directed
Wearing protective eyewear to avoid injuries
Limiting long-term use of steroid-based medications
Glaucoma is often hereditary, and having a family history significantly increases the risk of developing the condition. However, genes are only one part of the equation. Lifestyle, health conditions, and aging also influence how and when glaucoma develops. Whether or not you’ve inherited specific gene mutations, regular eye exams are key to early detection and timely management.
If you have concerns about hereditary glaucoma or are unsure about your personal risk, a conversation with an eye care provider can offer guidance. Through thorough evaluations and modern diagnostic tools, professionals can help identify risk factors and support your long-term vision needs.
If you’re looking for a screening, book an appointment at ProVision; they offer comprehensive eye health services tailored to patients with a family history of glaucoma and other vision conditions.