Synophthalmia is an extremely rare and severe birth defect in which the two eyes are fused into one or are so closely set that they appear as a single eye—this is usually part of the spectrum of holoprosencephaly, a disorder where the early embryonic forebrain fails to divide normally into right and left hemispheres. In synophthalmia, the brain’s midline structures are disrupted, and facial development is abnormal; in its most extreme form it overlaps with cyclopia, where there is a single central eye and often absence of a normal nose or presence of a proboscis. This condition arises very early in pregnancy (third to fourth week) during the formation of the prosencephalon, and it is usually incompatible with long-term survival because of profound brain and midline facial malformations.PMC Cleveland Clinic
Holoprosencephaly (HPE) is a congenital (present-at-birth) brain malformation in which the embryonic forebrain, called the prosencephalon, fails to divide completely into right and left hemispheres. Because the brain forms the scaffolding for the skull and facial midline, the condition can also disrupt eye, nose, and mouth development. Severity ranges from life-incompatible forms that merge almost the entire forebrain into one cavity to subtle “microforms” noticed only on a scan. The name combines three Greek roots—holos (whole), pros (front), and encephalon (brain)—and literally means “whole forebrain.” Most cases arise very early in pregnancy, often before many people realize they are pregnant, during the third to fifth gestational week when the neural tube is closing and regional brain patterning genes are switching on. Cleveland Clinic
In practical terms, HPE is not one single disease but a spectrum of structural brain differences with widely varying outlooks. Children with the mildest forms may grow into adulthood with manageable learning difficulties, whereas those with the most severe variant often die in utero or shortly after birth. NCBI
Why It Happens
Inside the embryo, sonic hedgehog (SHH) and related signaling molecules instruct the middle of the forebrain to split and create two symmetric cerebral hemispheres. A genetic glitch, toxic exposure, or metabolic imbalance can mute those signals. When the midline cells do not receive the correct “divide now” message, they stay fused, leaving a monoventricle (one fluid-filled space) and a single mass of cerebral tissue. Because facial tissues share the same molecular roadmap, the nose, eyes, and upper lip can fuse or misalign as well. The earlier and stronger the signaling disruption, the more dramatic the anatomic result. PMC
Major Types of Holoprosencephaly
Although many classification schemes exist, clinicians usually group HPE into four anatomic “types” arranged from most to least severe:
Alobar HPE – No visible separation of cerebral hemispheres; one large ventricle and absent interhemispheric fissure. Often linked with cyclopia or proboscis (rudimentary nose). Survival beyond the newborn period is extremely rare. Cleveland Clinic
Semilobar HPE – Partial but incomplete separation. The back part of the brain (occipital lobes) may split, yet the front remains fused. Microcephaly, seizures, and endocrine issues are common. Some infants survive but need intensive medical support. PMC
Lobar HPE – Almost complete separation except a short bridge of tissue in the frontal region; the corpus callosum is often small or absent. Children may have moderate learning disabilities yet can walk, talk, and attend school with supports. Cincinnati Children’s Hospital
Middle Interhemispheric Variant (MIHV, also called syntelencephaly) – An atypical pattern in which the center portions of the cerebral hemispheres stay fused but the front and back separate. Muscle tone problems and executive-function deficits are more noticeable than facial differences. NCBI
Microforms (e.g., single central incisor, subtle olfactory bulb fusion) sit at the mildest edge of the spectrum and may remain undetected until imaging is done for unrelated reasons.
Main Causes / Risk Factors
Holoprosencephaly is heterogeneous: sometimes a single gene mutation is enough; other times multiple environmental hits combine. Below are twenty well-documented causes or risk enhancers, each in plain language:
Chromosomal trisomy 13 (Patau syndrome) – Extra chromosome 13 disturbs dozens of developmental genes, making HPE the hallmark brain defect in this syndrome. NCBI
Trisomy 18 (Edwards syndrome) – Less common than in trisomy 13 but still significant, especially for semilobar forms.
Triploidy – Having an entire extra set of chromosomes is usually lethal and strongly associated with alobar HPE.
Single-gene SHH mutations – Faults in the SHH coding region blunt the key hedgehog signal that splits the forebrain.
ZIC2 mutations – This transcription factor guides neural tube patterning; variants can lead to MIHV without facial anomalies.
SIX3 mutations – A homeobox gene that orchestrates early eye and forebrain borders; loss-of-function variants yield lobar HPE.
Maternal pre-existing (type 1 or type 2) diabetes – High blood glucose injures embryonic neural crest cells; strict glycemic control lowers risk.
First-trimester alcohol exposure – Ethanol is a known teratogen; heavy binge episodes around week 3–4 multiply HPE odds.
Retinoic acid misuse (high-dose vitamin A derivatives) – Over-activation of RA signaling collapses forebrain segmentation.
Antiepileptic valproic acid – Disrupts folate pathways and histone acetylation, both critical in brain division.
TORCH infections (rubella, cytomegalovirus, toxoplasmosis) – Viral replication or inflammation may hinder prosencephalon cleavage.
Maternal phenylketonuria – Excess maternal phenylalanine alters neural tube differentiation unless diet is tightly managed.
Hypocholesterolemia – Cholesterol is required to activate SHH; very low maternal cholesterol states (e.g., Smith–Lemli–Opitz) impair signaling.
Consanguinity – Increases the chance of inheriting two faulty recessive alleles in HPE-associated genes.
Advanced maternal age (> 38 y) – Raises sporadic chromosomal non-disjunction events linked with trisomies.
Placental insufficiency and early hypoxia – Oxygen deprivation at critical weeks disrupts forebrain vascular patterning.
High-dose mycophenolate or methotrexate – Antimetabolite drugs interrupt rapidly dividing neural progenitors.
Maternal hyperthermia (e.g., prolonged fever, hot-tub exposure) – Sustained temperature > 102 °F during organogenesis damages midline cells.
Heavy metal exposure (e.g., mercury, lead) – Interferes with SHH and other morphogen gradients.
Unknown polygenic & multifactorial influences – In at least 40 % of cases, no single trigger is pinpointed, suggesting complex gene–environment interplay. Osmosis
Typical Signs & Symptoms
Microcephaly – Head size smaller than peers because cerebral volume is reduced.
Seizures – Disorganized cortex often fires abnormal electrical bursts, causing infantile spasms or focal seizures.
Developmental delay – Global milestones such as sitting, speaking, and social interaction occur later or need support.
Feeding difficulties – Poor suck-swallow coordination and oromotor dysfunction make weight gain hard.
Hypotonia or hypertonia – Muscle tone may be floppy or stiff depending on tract involvement.
Endocrine problems (diabetes insipidus, adrenal insufficiency) – Pituitary stalk malformation leads to hormone deficits.
Sleep–wake disturbance – Hypothalamic abnormalities scramble circadian regulation.
Temperature instability – Affected hypothalamic centers cannot fine-tune body temperature.
Cleft lip and/or palate – Failure of midline facial fusion mirrors the cerebral defect.
Single central incisor or absent nasal bridge – Facial “microform” flags mild brain fusion.
Cyclopia or proboscis – The most severe facial manifestation, almost exclusive to alobar HPE. Verywell Family
Hearing loss – Abnormal cranial nerve or ossicle development.
Visual impairment – Optic nerve hypoplasia or coloboma causes low vision or blindness.
Hydrocephalus – Impaired CSF flow can enlarge ventricles, raising intracranial pressure.
Autonomic dysregulation – Erratic heart rate, breathing pauses, or digestive motility issues due to brainstem immaturity. Cincinnati Children’s Hospital
Each child shows a unique blend; severity of brain fusion only loosely predicts daily functional challenges. Early physiotherapy, speech therapy, and endocrine replacement greatly improve quality of life for many survivors.
Diagnostic Tests
A. Physical-Exam–Based Tools
Comprehensive newborn neuro-dysmorphology exam – Neonatologists inspect craniofacial midline, palate, limb tone, and reflexes; subtle clues such as a single maxillary central incisor may trigger imaging.
Head circumference measurement – Serial plotting detects microcephaly or macrocephaly due to hydrocephalus.
Ocular exam with ophthalmoscope – Reveals optic nerve hypoplasia, colobomas, or fused globes.
Growth and endocrine status charting – Regular weight/length tracking plus skin turgor, thirst, and polyuria review raise suspicion for pituitary hormone loss.
B. Manual / Bedside Functional Tests
- Developmental milestone screening (e.g., Denver II) – Quickly identifies gross motor, fine motor, language, and social delays suggestive of structural brain abnormalities.
- Cranial nerve assessment – Checking eye movements, facial symmetry, gag reflex, and hearing helps localize midline anomalies.
- Manual muscle tone scoring (Modified Ashworth or Tardieu) – Quantifies spasticity or flaccidity guiding early therapy plans.
C. Laboratory & Pathological Tests
- Standard karyotype – Detects trisomy 13, 18, triploidy, or large translocations.
- Chromosomal microarray – Finds micro-deletions or duplications too small for karyotype, such as 7q36 deletion containing SHH.
- Targeted gene panel / whole-exome sequencing – Screens dozens of single-gene culprits (SHH, ZIC2, SIX3, TGIF1, etc.); helps with prognosis and future pregnancy planning. PMC
- Maternal hemoglobin A1c – Retrospective clue for poorly controlled diabetes in prenatal cases.
- Serum electrolytes & serum/urine osmolality – Evaluates diabetes insipidus or adrenal insufficiency secondary to pituitary disruption.
D. Electrodiagnostic Tests
- Electroencephalogram (EEG) – Captures seizure activity patterns; hypsarrhythmia may appear in infants with severe cortical disorganization.
- Brainstem auditory evoked responses (BAER) – Assesses integrity of auditory pathways if structural imaging shows temporal-lobe malformation.
- Visual evoked potentials (VEP) – Complements ophthalmologic exam, quantifying optic nerve conduction when infants cannot cooperate with vision charts.
E. Imaging Tests
- Prenatal ultrasound (first-trimester nuchal & anatomy scans) – The most common first clue; absent “butterfly” midline or single ventricle prompts referral. AJR Online
- In-utero fetal MRI – Provides high-resolution images safe for mother and fetus, detailing brain structure and guiding delivery counseling. AJNR
- Postnatal brain MRI – Gold standard for subtype classification; clarifies whether corpus callosum bridges and identifies treatable hydrocephalus.
- Head CT – Rapid bedside alternative in unstable neonates; shows calcifications or bony midline defects.
- 3-D craniofacial CT or stereophotogrammetry – Maps facial bone relationships for surgeons planning cleft or nasal reconstruction. Child Neurology Foundation
Non-Pharmacological Treatments
Because synophthalmia is structural and developmental, there is no cure; care centers on supportive, multidisciplinary, non-drug interventions to maximize comfort, function if possible, and family support. Each below is described with purpose and mechanism in simple terms:
Multidisciplinary Care Coordination – A team (neurology, genetics, endocrinology, nutrition, surgery, palliative care) works together so all problems are seen and managed in a unified plan. Purpose: avoid fragmented care. Mechanism: regular team meetings and a lead care coordinator smooth decision-making.PMC
Genetic Counseling – Educating and testing the family about recurrence risk, underlying mutations, and implications for future pregnancies. Purpose: informed family planning. Mechanism: review family history, offer genetic testing, explain inheritance.PMCPMC
Prenatal Diagnosis and Early Decision Support – Using high-resolution ultrasound and fetal MRI to detect synophthalmia/holoprosencephaly early in pregnancy. Purpose: prepare parents, consider options. Mechanism: imaging evaluates brain midline development.Cleveland ClinicChild Neurology Foundation
Feeding Support (e.g., NG/Gastrostomy Tubes) – Many infants have trouble sucking/swallowing; placing feeding tubes ensures proper nutrition. Purpose: prevent malnutrition. Mechanism: direct delivery of calories and fluids bypassing ineffective oral feeding.NCBI
Respiratory Support and Airway Management – Some babies have airway obstruction or underdeveloped facial structures; non-invasive ventilation or tracheostomy when needed. Purpose: keep airway open and oxygen levels safe. Mechanism: mechanical assistance with breathing.NCBI
Seizure Precautions and Monitoring (Non-Drug Environment) – Many affected infants develop seizures; creating a safe environment, seizure detection devices, and caregiver training reduces injury. Purpose: reduce risk from uncontrolled seizures. Mechanism: remove sharp objects, padded bedding, training in seizure first aid.NCBI
Developmental Stimulation and Early Intervention – Occupational, speech, and sensory therapy to maximize any possible developmental gains. Purpose: support neurodevelopment and skill acquisition. Mechanism: guided play, exercises, and stimulation tailored to the child’s ability.PMC
Physical Therapy – Helps with muscle tone, positioning, and mobility to prevent contractures and improve comfort. Purpose: maintain function and reduce pain. Mechanism: stretching, positioning, passive movement.PMC
Occupational Therapy – Focuses on daily living adaptation, feeding strategies, and sensory processing. Purpose: increase independence or ease of care. Mechanism: training caregivers, adaptive tools, and activity modification.PMC
Vision and Hearing Evaluation & Adaptive Support – Even with severe ocular malformations, assessing any residual vision/hearing guides use of aids. Purpose: tailor environmental cues. Mechanism: low-vision aids, alternative communication techniques.Cleveland Clinic
Craniofacial and Prosthetic Evaluation – For surviving infants, planning reconstructive or cosmetic assistance (e.g., for clefts or midline facial defects). Purpose: improve feeding, airway, and appearance. Mechanism: prosthetics or staged soft-tissue preparation.PMC
Palliative Care and Comfort Measures – Focus on quality of life, symptom relief, and family support when cure is not possible. Purpose: reduce suffering. Mechanism: pain assessment, comfort positioning, psychological support.PMC
Family Psychological Counseling – Helping parents cope with grief, stress, and decision-making. Purpose: emotional resilience. Mechanism: structured therapy, support groups.PMC
Social Work and Resource Navigation – Assist families with access to services, insurance, and home care. Purpose: reduce logistical burdens. Mechanism: advocacy and linking to community resources.PMC
Adaptive Equipment and Positioning Devices – Special chairs, cushions, or supports to keep the child safe and comfortable. Purpose: prevent pressure sores, ease feeding. Mechanism: ergonomic devices customized to anatomy.PMC
Seizure Detection Technologies (e.g., Wearables) – Non-pharmacologic monitoring to alert caregivers of events. Purpose: faster response. Mechanism: sensors detecting movement or autonomic changes.NCBI
Educational Planning (if survival permits) – Early planning for schooling or special education tailored to cognitive ability. Purpose: maximize learning potential. Mechanism: individualized education programs.PMC
Nutritional Counseling for Caregivers – Guidance on caloric needs, consistency of feeds, and managing fluid balance especially if endocrine issues exist. Purpose: prevent over/under hydration. Mechanism: tailored feeding plans.PMCNCBI
Environmental Enrichment and Sensory Input – Safe tactile and auditory stimulation to support any preserved brain function. Purpose: encourage engagement. Mechanism: light, sound, touch in controlled ways.PMC
Advance Care Planning – Early discussions on goals of care, resuscitation preferences, and end-of-life decisions if prognosis is poor. Purpose: align medical care with family values. Mechanism: structured family meetings.PMC
Drug Treatments
There is no drug that reverses synophthalmia itself; medications treat complications (seizures, endocrine dysfunction, fluid imbalance). Below are commonly used classes with typical examples, dosing principles (pediatric dosing must be individualized by specialists), timing, and key side effects:
Levetiracetam (Antiepileptic) – Class: pyrrolidine derivative. Used for seizures common in holoprosencephaly. Typical starting dose in infants: 10 mg/kg twice daily, can titrate up to 60 mg/kg/day. Purpose: reduce seizure frequency. Mechanism: modulates synaptic neurotransmitter release via SV2A binding. Side effects: irritability, sleepiness, behavioral changes.Medscape
Valproic Acid (Antiepileptic) – Class: broad-spectrum anticonvulsant. Dosage: often starts around 10–15 mg/kg/day, titrated to effect. Purpose: seizure control. Mechanism: increases GABA availability and modulates ion channels. Side effects: liver toxicity, weight gain, thrombocytopenia, pancreatitis. Use with caution in infants.Medscape
Phenobarbital (Antiepileptic) – Class: barbiturate. Commonly used neonatal seizure drug. Dosage: loading 20 mg/kg, maintenance 3–5 mg/kg/day. Purpose: acute and chronic seizure control. Mechanism: enhances GABAergic inhibition. Side effects: sedation, respiratory depression, cognitive slowing.Medscape
Desmopressin (DDAVP) – Class: vasopressin analog. Used if central diabetes insipidus develops (common endocrine issue). Dosage: nasal or low-dose injection, individualized (e.g., 0.05–0.1 mcg/kg). Purpose: reduce excessive urination and dehydration. Mechanism: acts on renal V2 receptors to concentrate urine. Side effects: hyponatremia if overused.PMCPMC
Levothyroxine – Class: thyroid hormone replacement. Indicated in central hypothyroidism. Dosage: weight-based (e.g., ~10–15 mcg/kg/day in infants, adjusted). Purpose: normalize metabolism, growth. Mechanism: synthetic T4 replaces deficient thyroid hormone. Side effects: over-replacement can cause irritability, tachycardia.PMCPMC
Hydrocortisone – Class: glucocorticoid. Used for central adrenal insufficiency. Dosage: physiologic replacement (~8–12 mg/m²/day total, divided). Purpose: support stress response, blood pressure. Mechanism: replaces cortisol. Side effects: weight gain, immune suppression if high doses.PMCPMC
Growth Hormone (Recombinant) – Class: endocrine therapy. Used if growth hormone deficiency identified. Dosage: individualized per endocrinologist, often ~0.025–0.05 mg/kg/day subcutaneously. Purpose: support growth and metabolism. Mechanism: stimulates IGF-1 production and growth processes. Side effects: joint pain, increased intracranial pressure (rare).PMCPMC
Antireflux Medications (e.g., H2 blockers or Proton Pump Inhibitors) – Class: acid suppression (e.g., ranitidine historically, now alternatives like famotidine or omeprazole under careful dosing). Purpose: prevent esophagitis from reflux, common in neurologically impaired infants. Mechanism: reduce gastric acidity. Side effects: altered gut flora, potential increased infection risk.NCBI
Antibiotics (Targeted) – Class: variable. Used for secondary infections (e.g., aspiration pneumonia). Purpose: treat bacterial infections. Mechanism: bacterial eradication. Side effects: depending on agent—GI upset, allergy, resistance. (Use after culture when possible.)NCBI
Electrolyte and Fluid Management Solutions – While not a “drug” in classical sense, careful use of intravenous fluids or electrolyte replacement is medical therapy for dehydration from diabetes insipidus or endocrine imbalance. Purpose: keep internal balance. Mechanism: replace sodium, water per tailored protocols. Side effects: overcorrection can cause seizures or edema.PMCNCBI
Dietary Molecular Supplements
Most of these are more relevant for prevention in pregnancy or general support in early development; evidence specific to synophthalmia is limited, so they are used to support brain development, reduce risk, or improve overall health.
Folic Acid (Vitamin B9) – Dosage: 400–800 mcg daily preconception and first trimester (higher risk families may use 4–5 mg). Function: supports DNA synthesis and midline neural development. Mechanism: methylation pathways critical to early neural tube and forebrain formation. Supplementation reduces risk of some midline defects.PMCMDPI
Choline – Dosage: ~450 mg/day (pregnant women). Function: supports brain development. Mechanism: methyl donor in neurogenesis and membrane synthesis. Emerging evidence indicates benefits for fetal brain structure.PMC
Vitamin B12 – Dosage: 2.6 mcg/day (pregnancy) or supplementation if deficient. Function: supports neural development and works with folate. Mechanism: methylation and myelin maintenance. Deficiency can impair brain development.MDPI
Omega-3 Fatty Acids (DHA/EPA) – Dosage: ~200–300 mg DHA daily in pregnancy/early life. Function: supports neuronal membrane integrity and cognitive development. Mechanism: incorporated into brain phospholipids, modulates inflammation.PMC
Vitamin D – Dosage: 600–800 IU daily (adjust per levels). Function: bone health and immune modulation. Mechanism: nuclear receptor signaling affecting neurodevelopment indirectly. Deficiency is common in vulnerable infants.PMC
Zinc – Dosage: ~11 mg/day in pregnancy (adjust if deficiency). Function: immune support and growth. Mechanism: cofactor in hundreds of enzymes including those involved in development. Zinc deficiency has been linked to congenital anomalies.PMC
Iron – Dosage: pregnancy iron supplementation per anemia status (typically 27 mg elemental). Function: prevents maternal anemia and supports oxygen delivery. Mechanism: critical for brain oxygenation and development.PMC
Probiotics – Dosage: varies by formulation. Function: gut health to improve nutrient absorption and immune balance. Mechanism: modulate microbiome, reduce systemic inflammation that might stress development. Evidence is general and not disease-specific.PMC
Antioxidants (e.g., Vitamin C) – Dosage: ~85 mg/day pregnant. Function: reduces oxidative stress. Mechanism: neutralizes free radicals that could damage developing tissues. No direct proof prevents synophthalmia but supports healthy gestation.PMC
Medium-Chain Triglycerides (MCT Oil) – Dosage: as part of high-calorie formula under dietitian guidance. Function: easy energy for infants with feeding difficulties. Mechanism: rapidly absorbed fats bypass typical digestion, supporting weight.NCBI
Note: All supplementation should be guided by a clinician; excess (especially vitamin A) can be harmful in pregnancy, so avoid high-dose retinoids unless prescribed.PMC
Regenerative / Stem Cell or Experimental Approaches
There are no approved regenerative or stem-cell “cures” for synophthalmia or the underlying severe holoprosencephaly. The following are experimental or theoretical approaches under investigation in related neuro- or ocular developmental disorders. They must be framed as investigational, with unclear benefit and unknown long-term safety:
Neural Stem Cell Transplantation (Experimental) – Function: potential to replace or support malformed neural tissue. Mechanism: transplanted progenitor cells could integrate or secrete trophic factors. Status: preclinical; major challenges in guiding correct midline brain patterning.PMCPMC
Induced Pluripotent Stem Cell (iPSC)-Derived Neural Cells – Function: patient-specific cell modeling and potential future therapy. Mechanism: reprogrammed cells differentiated into neural types for transplantation or disease modeling. Limitations: integration, tumor risk, and correct organization remain unsolved.PMCAmerican Academy of Ophthalmology
Mesenchymal Stem Cell (MSC) Therapy (Paracrine / Neuroprotection) – Function: modulate inflammation and secrete protective factors for surrounding tissue. Mechanism: MSCs release cytokines and exosomes that support survival, not direct structural correction. Status: early phase in neurologic disease; unproven for holoprosencephaly.PMCPMC
Exosome-Based Neurotrophic Therapies – Function: deliver regenerative signals without whole cells. Mechanism: exosomes carry microRNA and proteins that influence cell survival and differentiation. Research is emerging in ocular and brain injury settings.PMCMDPI
Gene Therapy Targeting SHH or Related Pathways (Highly Experimental) – Function: correct upstream signaling defects. Mechanism: vector delivery to adjust Hedgehog pathway expression in early development (theoretically). Currently not feasible in humans for midline embryonic defects.PMC
Retinal or Ocular Tissue Engineering (Related to Cyclopia/Visual Support) – Function: future vision restoration research in retinal diseases offers insight into reconstructive possibilities. Mechanism: combining scaffolds, stem cells, and growth factors to rebuild ocular structures. Not directly applicable to synophthalmia’s fused-eye anatomy but informs the regenerative field.MDPI
Important caveat: All of the above are investigational; no standard dosing exists, and they are not standard care. Families should only consider them within approved clinical trials.PMCAmerican Academy of Ophthalmology
Surgical Procedures (What They Are and Why Done)
Ventriculoperitoneal (VP) Shunt – Procedure: install a drain from brain ventricles to the abdomen. Why: relieve hydrocephalus (fluid buildup in the brain), which is common in holoprosencephaly and can cause pressure, vomiting, or worsening neurologic status.NCBI
Feeding Tube Placement (Gastrostomy or NG Tube) – Procedure: place a tube directly into the stomach or nose for feeding. Why: many infants cannot feed orally due to neurological and facial malformations; this ensures adequate nutrition.NCBI
Tracheostomy – Procedure: create a hole in the neck into the windpipe for breathing. Why: bypass upper airway obstruction from facial anomalies or to provide long-term ventilation support.NCBI
Craniofacial Reconstruction / Cleft Repair – Procedure: surgical correction of midline facial clefts or other structural defects. Why: improve feeding, airway, and appearance when survival allows staged reconstruction.PMC
Palliative Surgical Procedures (e.g., soft tissue adjustments for comfort) – Procedure: minor surgeries to ease care, such as releasing tight tissues causing discomfort. Why: improve quality of life when curative surgery is not possible.PMC
Preventions (Primarily for Future Pregnancies)
Preconception Folic Acid Supplementation – Start before pregnancy to reduce risk of holoprosencephaly and midline defects.MDPI
Good Diabetes Control in the Mother – High blood sugar early in pregnancy increases risk; tight control lowers it.PMC
Avoidance of Known Teratogens (e.g., Isotretinoin, Alcohol) – These can disrupt early brain patterning; avoid especially in first trimester.PMC
Genetic Counseling if Family History Exists – Identify carriers or inherited mutations to assess recurrence risk and consider testing.PMC
Early and Regular Prenatal Care with High-Resolution Imaging – Detect anomalies early for decision-making and planning.Cleveland ClinicChild Neurology Foundation
Avoid Maternal Smoking and Environmental Toxins – Reduce exposures that might synergize with genetic predispositions.PMC
Maintain Healthy Maternal Weight and Nutrition – Obesity and poor nutrition can affect early development.PMC
Vaccination and Infection Prevention (TORCH Pathogens) – Avoid maternal infections that could stress embryogenesis.PMC
Review Medications with Provider Before Pregnancy – Ensure none are teratogenic or modifiable.PMC
Folate-Rich Diet (Dark Greens, Beans, Fortified Grains) Alongside Supplement – Natural support for neural development.MDPI
When to See a Doctor
Prenatal ultrasound shows brain midline abnormalities or fused facial features.Cleveland ClinicChild Neurology Foundation
Newborn has abnormal head or face shape (single eye area, missing nose, cleft).PMC
Difficulty breathing or airway obstruction signs.NCBI
Feeding failure, poor sucking, or failure to thrive.NCBI
Seizures or unusual movements.NCBI
Excessive urination/dehydration suggesting diabetes insipidus.PMC
Signs of hormone imbalance (lethargy, low blood pressure, poor growth).PMC
Recurrent infections or unexplained fever.NCBI
Developmental stagnation in surviving infants.PMC
Family considering another pregnancy—preconception genetic counseling.PMC
What to Eat and What to Avoid
- For Pregnant Mothers (Prevention Focus):
Eat a diet rich in folate (leafy greens, beans, fortified grains), choline (eggs, legumes), omega-3s (fish low in mercury), vitamin B12 (meat, dairy, or supplement if vegetarian), and adequate iron and zinc. Avoid alcohol, isotretinoin, unconsulted herbal supplements, and high-dose vitamin A (retinoids) which can be teratogenic. Manage blood sugar and avoid smoking.MDPIPMC - For Affected Infants (Supportive Nutrition):
Provide high-calorie, easy-to-swallow formulations via feeding tubes if needed, ensure balanced micronutrients (vitamin D, iron for anemia prevention), and monitor fluid balance carefully if endocrine issues like diabetes insipidus are present (avoid free unrestricted water without medical guidance). Avoid choking hazards and foods that are hard to chew or swallow.NCBIPMC
Frequently Asked Questions (FAQs)
What is synophthalmia?
Synophthalmia is a rare birth defect where the eyes are fused or too close together, usually part of severe brain malformations known as holoprosencephaly.PMCWhy does synophthalmia happen?
It happens due to genetic changes or environmental insults early in pregnancy that disrupt the normal division of the forebrain and midline facial development.PMCPMCCan synophthalmia be cured?
No. There is currently no cure; treatment focuses on managing symptoms and supporting quality of life.PMCIs it inherited?
Sometimes; mutations in certain genes can be passed on, but many cases are sporadic. Genetic counseling helps assess risk.PMCPMCHow is it diagnosed before birth?
High-resolution ultrasound and fetal MRI during early pregnancy can detect brain and facial midline defects.Cleveland ClinicChild Neurology FoundationWhat happens after birth?
Newborns often need breathing support, feeding help, seizure monitoring, and hormonal evaluation. Many have a poor long-term prognosis depending on severity.NCBIPMCCan children with synophthalmia develop normally?
Most have significant neurologic impairments; only mild or atypical forms (rare) may allow some development with intensive support.PMCAre there medications that fix the defect?
No. Medications only treat complications like seizures or hormone deficiencies.MedscapeCan future pregnancies be safer?
Yes, with preconception counseling, folic acid, good diabetes control, avoiding teratogens, and early screening.MDPIPMCIs stem cell therapy a cure?
Not today. Stem cell and regenerative approaches are experimental and have not proven effective for this condition.PMCAmerican Academy of OphthalmologyWhat specialists will be involved?
Neonatologists, neurologists, geneticists, endocrinologists, surgeons, nutritionists, therapists, and palliative care.PMCWhat support can families get?
Genetic counseling, psychological services, social work, early intervention programs, and palliative care for decision support.PMCIs prenatal testing available to know the cause?
Yes. Genetic panels, chromosomal microarrays, or sequencing can sometimes identify underlying mutations.PMCWhat is the life expectancy?
It varies; severe forms often result in death in infancy, while milder variants (if truly synophthalmia and not complete cyclopia) may survive longer but with disabilities.PMCCan siblings be tested or screened?
Yes. If a familial mutation is found, siblings or future embryos (with IVF) can be evaluated.PMC
Disclaimer: Each person’s journey is unique, treatment plan, life style, food habit, hormonal condition, immune system, chronic disease condition, geological location, weather and previous medical history is also unique. So always seek the best advice from a qualified medical professional or health care provider before trying any treatments to ensure to find out the best plan for you. This guide is for general information and educational purposes only. Regular check-ups and awareness can help to manage and prevent complications associated with these diseases conditions. If you or someone are suffering from this disease condition bookmark this website or share with someone who might find it useful! Boost your knowledge and stay ahead in your health journey. We always try to ensure that the content is regularly updated to reflect the latest medical research and treatment options. Thank you for giving your valuable time to read the article.
The article is written by Team RxHarun and reviewed by the Rx Editorial Board Members
Last Updated: August 01, 2025.
Synophthalmia
