

Many parents are surprised after their baby is born to notice that the size of the eye doesn’t look normal, and the first question that comes to mind is: “Does my child have a problem?”
One of the most common conditions that can appear early is Microphthalmia (small eye) in children. This condition may have different causes—sometimes genetic, other times due to issues during pregnancy.Microphthalmia can affect the shape of the eye, vision, and even the child’s self-esteem as they grow up.???? In this Daleely Medical guide, we’ll explain the main causes of microphthalmia, the symptoms parents should look out for, how the condition is diagnosed, the latest treatment options (whether through exercises or surgery), and the most important tips to help your child live a normal and confident life.
Microphthalmia is a congenital condition where the eyeball is smaller than normal. It can affect one eye or both eyes.
Yes. In most cases, vision is very weak or absent, but in some children there may be a small amount of usable vision.
Genetic factors.
Maternal infections during pregnancy, such as rubella or toxoplasmosis.
Exposure to harmful substances or medications during pregnancy.
Abnormal eye development in the fetus.
No. The eye does not grow to a normal size, which makes it different from temporary eye problems that may improve with age.
Using eye expanders to prepare the socket.
Cosmetic artificial eye (ocular prosthesis).
Surgical procedures to enlarge the socket or adjust the eyelids.
Vision therapy and exercises if there is any remaining vision.
Exercises do not increase eye size, but they help strengthen eye muscles, stimulate any existing vision, and support coordination.
It can be genetic. That’s why doctors sometimes request genetic testing to confirm the cause.
Yes ✅ With early treatment (especially cosmetic intervention) and family support, children can live a normal and confident life.
The earlier the intervention (from the first months of life), the better the results for eye socket growth and facial symmetry.
Like any surgery, there is a risk of partial failure or complications. However, regular follow-ups with a pediatric ophthalmic surgeon greatly reduce the risks.
No.
Atrophy: the eye is normal at birth but shrinks or loses function later.
Microphthalmia: the eye is small from birth (a congenital defect).
Yes, an artificial eye is used for cosmetic purposes to restore natural appearance, but it does not provide vision.
Yes ✅ As the child grows, the prosthesis must be replaced or adjusted to match facial bone development.
No, the other eye is usually normal. However, it must be protected and checked regularly to avoid extra strain or injury.
CT scan or MRI to assess the eye and orbit size.
Genetic tests if a hereditary cause is suspected.
Yes, but it’s best to avoid contact sports with strong facial impact (e.g., boxing).
Yes. A small eye may affect the growth of surrounding bones, which is why early socket expansion and cosmetic treatment are important.
Unfortunately, yes.
Solutions: early cosmetic treatment, family support, and boosting the child’s self-confidence.
It’s not very common, but doctors are now more experienced in early diagnosis and management.
One eye: the child relies mostly on the healthy eye.
Both eyes: vision is often very weak or absent, making the condition more challenging.
Genetic factors
Mutations in genes responsible for eye formation.
May appear as an isolated case or part of syndromes such as CHARGE or Walker-Warburg.
Problems during pregnancy
Maternal infections: rubella, toxoplasmosis, herpes.
Exposure to radiation, chemicals, or harmful drugs.
Fetal development disorders
Abnormal development of the neural tube or eye tissues.
Reduced blood supply or oxygen during pregnancy.
Associated eye conditions
Congenital retinal detachment.
Lens–cornea adhesion.
Corneal or lens opacity.
Unknown causes
Sometimes the condition is classified as unexplained congenital anomaly.
Eye smaller than normal, visible compared to the other eye or peers.
Eye deformity: sunken or bulging appearance.
Poor vision (degree depends on severity).
Strabismus (squint) due to size or vision difference.
Frequent tearing or discharge (blocked tear ducts).
Sometimes linked to other developmental disorders.
Mild Microphthalmia
Slightly smaller eye, sometimes unnoticed until later.
Moderate/Complex Microphthalmia
Smaller eye + other eye problems (corneal opacity, retinal issues, congenital glaucoma).
Severe Microphthalmia
Very small, underdeveloped eye with little or no vision.
Requires cosmetic or surgical intervention.
Partial Anophthalmia
Eye extremely small, almost absent.
Different from complete anophthalmia, but with similar vision loss.
Unlike diseases that progress, microphthalmia is classified into levels:
Stage 1 (Mild): Slightly smaller eye, near-normal vision possible.
Stage 2 (Moderate): Noticeably small eye, strabismus, reduced vision.
Stage 3 (Severe): Very small, incomplete eye, vision almost absent.
Stage 4 (Partial Anophthalmia): Eye extremely small, almost invisible, no vision.
Vision loss: mild to complete blindness depending on severity.
Strabismus & amblyopia (lazy eye).
Psychological & social effects: bullying, low self-esteem.
Facial bone development issues: asymmetry due to poor orbital growth.
Associated syndromes: may come with brain, heart, or hearing problems.
Poor vision or a noticeable size difference between the eyes increases the risk of strabismus (crossed eyes).
Over time, the weaker eye may develop amblyopia (lazy eye), where the brain stops relying on it.
The different eye appearance may lead to bullying or embarrassment.
This can affect the child’s confidence and social interactions.
A small eye can impact the growth of the orbital bones (eye socket).
This may cause facial asymmetry.
Sometimes microphthalmia appears alongside other congenital problems, such as heart defects, brain abnormalities, or hearing loss (especially if it’s part of a genetic syndrome).
That’s why a child often needs care from a multidisciplinary team, not just an eye specialist.
Early diagnosis is crucial for planning treatment. Doctors use several methods:
The ophthalmologist compares eye size with normal measurements for the child’s age.
They examine the cornea, lens, retina, and eye movements.
Ultrasound imaging accurately measures eye size.
It also detects internal abnormalities such as retinal detachment or lens opacity.
Used in severe or complex cases.
Shows details of the small eye, surrounding orbit, and bone structure.
Depending on the child’s cooperation, simple tests are used to evaluate sight.
Continuous follow-up is essential to track any remaining vision.
Ordered if a genetic syndrome is suspected.
May include DNA tests, plus brain, heart, and hearing assessments.
❌ Currently, there are no eye drops or medications that make the eye grow normally, since the condition is congenital.
However, medications are used to manage complications:
Eye drops for glaucoma if present.
Anti-inflammatory drops or ointments.
Antibiotics for recurrent infections.
Glasses or contact lenses to improve remaining vision.
Goal: enlarge the orbit and stimulate bone growth.
Method: gradually adjustable orbital expanders.
Done in stages with long-term follow-up.
Used when the eye is very small and has no vision.
Purpose: cosmetic improvement + maintaining facial bone growth.
Needs replacement as the child grows.
Placed in the socket instead of the small or absent eye.
Provides facial volume.
Later, a prosthetic eye can be fitted over it.
Corrects drooping or asymmetry of the eyelids.
Makes the small eye or prosthesis look more natural.
Cataract removal.
Retinal detachment repair.
Glaucoma treatment.
Goal: preserve any remaining vision.
Despite generally good results, some surgeries may fail due to:
Poor response of orbital tissue or bones (orbit doesn’t expand properly).
Implant rejection (inflammation or implant displacement).
Healing complications (chronic infections, discharge, or tissue erosion).
Cosmetic issues (prosthesis not matching the other eye, eyelid asymmetry).
Growth-related changes (children outgrow implants/prostheses, requiring adjustments).
Persistent cosmetic differences (asymmetry between eyes).
Facial bone growth abnormalities.
Chronic pain or infections.
Emotional frustration for both child and parents.
Choose an experienced pediatric oculoplastic surgeon.
Maintain regular follow-ups after surgery.
Replace prostheses or expanders as advised.
Follow post-op care instructions carefully.
Regular medical follow-up: with pediatric ophthalmologists; complex cases may need a geneticist and oculoplastic surgeon.
Adherence to treatment: use prescribed glasses, drops, or prosthesis care routines.
Early intervention: the earlier the treatment, the better the cosmetic and developmental outcomes.
Psychological support: reassure the child, prevent bullying, and seek therapy if needed.
Cosmetic care: prostheses and eyelid surgeries are essential for appearance and confidence.
Infection prevention: maintain hygiene of prostheses/implants; seek medical help if redness or discharge appears.
Prepare for adjustments with growth: changing prostheses or expanders as the child grows is normal, not a treatment failure.
Important note: Microphthalmia is a congenital condition; exercises cannot enlarge the eye.
Their role is to:
Improve movement of the existing eye.
Stimulate eye and eyelid muscles.
Strengthen the healthy eye.
Support visual-motor coordination.
Eye Muscle Strengthening
Child focuses on a near object (toy) for 10 seconds.
Then shifts focus to a distant object.
Repeat 5–10 times daily.
Eye Movement Training
Use a toy or small light moving up, down, right, and left.
Child follows the movement to activate eye muscles.
Patch Therapy
Covering the healthy eye for specific hours daily (if the small eye has some vision).
Encourages use of the weaker eye.
Magnifier-Based Focus Training
Using magnifying glasses or puzzle/reading activities with fine details.
Enhances visual effort in the weaker eye.
Visual-Motor Coordination Games
Activities like throwing/catching a ball, building blocks, or maze games.
Improve eye-body coordination.
⚠️ Important Notes
Exercises are supportive, not a substitute for surgery or prosthesis.
Must be guided by a pediatric ophthalmologist or vision therapist.
Consistency is more important than duration.
The goal is better function, not increasing eye size.