
When a question is raised about your baby's brain on routine scanning, fetal neurosonography provides the detailed, specialist-level answer — examining structure, development, and anatomy plane by plane.
Fetal neurosonography is a specialist ultrasound examination of the fetal brain and central nervous system that goes considerably deeper than the brain assessment included in a standard anomaly scan. While the anomaly scan screens for major brain abnormalities, neurosonography examines the developing brain in fine anatomical detail — plane by plane, structure by structure.
It is performed by Dr. Kunda Shahane on the GE Voluson Signature Expert, using dedicated neurosonography protocols with high-frequency transducers and, where needed, transvaginal imaging for optimal views of posterior fossa structures.
It is typically requested when a finding has been identified on a routine anomaly scan — or when there is a clinical risk factor that warrants a more thorough examination of the fetal brain and spine.
| Also called | Fetal brain scan · Fetal neurosonogram |
| Optimal timing | 24–28 weeks (possible 20–32 wks) |
| Duration | 45–90 minutes |
| Risk to baby | None — standard ultrasound |
| Machine | GE Voluson Signature Expert |
| Performed by | Dr. Kunda Shahane, FIFM |
| Fetal MRI needed? | In selected cases — Dr. Kunda will advise |
Fetal neurosonography evaluates every major brain structure — well beyond what a routine anomaly scan covers. Each structure below is examined systematically.
Sulcal and gyral development — the surface folding of the brain, which follows a precise gestational timetable
Complete, partial, or absent — this white matter bridge between hemispheres is assessed in full across all segments
Size and symmetry of the fluid-filled spaces — ventriculomegaly is the most common brain finding requiring neurosonography
Cerebellum, vermis, 4th ventricle, and cisterna magna — assessed for Dandy-Walker malformation and cerebellar abnormalities
Site of neuronal production and a common location for haemorrhage in premature infants — assessed for cysts and bleeding
Deep grey matter structures — their morphology and echogenicity are assessed for structural and metabolic conditions
Colour Doppler assessment of cerebral vascular anatomy — detecting arteriovenous malformations and vascular anomalies
Complete cervical, thoracic, lumbar, and sacral spine assessment for spina bifida, sacral agenesis, and cord tethering
Fluid collections outside brain parenchyma — classified by location, size, and likely clinical significance
| Condition | What It Means | Severity |
|---|---|---|
| Mild Ventriculomegaly | Lateral ventricle 10–12mm — common finding; often isolated and resolves. Requires detailed assessment and follow-up. | Variable |
| Moderate / Severe Ventriculomegaly | Ventricle >12mm — higher risk of associated findings. Chromosomal testing and MRI often recommended. | Significant |
| Agenesis of Corpus Callosum | Complete or partial absence of the corpus callosum — can be isolated or associated with syndromes. Outcome varies widely. | Variable |
| Dandy-Walker Malformation | Posterior fossa anomaly with enlarged 4th ventricle, cystic space, and vermian abnormality. Often requires specialist counselling. | Significant |
| Holoprosencephaly | Failure of the forebrain to divide — ranges from alobar (severe) to microform. Associated with chromosomal abnormalities. | Severe |
| Neural Tube Defects (Spina Bifida) | Open or closed defects of the spine — from open spina bifida (myelomeningocele) to sacral agenesis. | Significant |
| Intracranial Haemorrhage | Bleeding within the fetal brain — detected as hyperechoic areas. Cause determines prognosis. Requires prompt evaluation. | Urgent |
| Arachnoid Cysts | Fluid-filled cysts outside brain tissue — most are benign and isolated, but location and size determine significance. | Often benign |
| Subependymal Cysts | Small cysts in the germinal matrix area — usually resolving. Some patterns associated with CMV infection. | Usually benign |
| Cerebral Cortical Dysplasia | Abnormal cortical folding — lissencephaly (smooth brain) or polymicrogyria (over-folded). Limited detection before 28 weeks. | Significant |
Fetal neurosonography and fetal MRI are complementary. MRI may be advised when ultrasound views are suboptimal due to fetal position or maternal habitus, when complex cortical development abnormalities are suspected (e.g. lissencephaly, polymicrogyria), or when the corpus callosum or posterior fossa findings need further characterisation. Dr. Kunda Shahane will advise whether MRI adds value in your specific case, and can coordinate the referral.
Dr. Kunda reviews your anomaly scan report, referral note, and clinical history before the scan begins. She explains what the scan aims to answer and what findings she will be looking for.
The scan is performed through the abdomen using the GE Voluson Signature Expert. Each brain structure is imaged in standardised planes — axial, coronal, and sagittal — with measurements taken and documented. If fetal position limits views, transvaginal ultrasound may be used for better posterior fossa visualisation.
Blood flow assessment of the Circle of Willis and middle cerebral artery is performed where indicated — particularly if an arteriovenous malformation or vascular anomaly is suspected.
The entire spine is imaged in longitudinal and transverse planes — from cervical to sacral — to detect open or closed neural tube defects and structural anomalies.
After the scan, Dr. Kunda discusses findings with you in detail — what has been seen, what it means, what further investigations or follow-up are needed, and what the evidence says about outcomes. You leave with a written report and a clear next step.
"The fetal brain is the most complex and the most humbling structure I examine. A measurement of 11mm in a lateral ventricle can mean many different things — and getting that distinction right requires not just the right machine, but the right experience with the right protocols. My commitment to every family who comes for neurosonography is this: I will look at every structure, document every measurement, and tell you exactly what I see — with honesty about what we know, and equal honesty about what we do not yet know."— Dr. Kunda Shahane, MBBS, MS (Obs & Gynae), FIFM, FMF (London)
Send your anomaly scan report on WhatsApp and we will confirm your appointment within hours.
Mayflower Fetal Medicine Centre strictly complies with the PCPNDT Act, 1994. All ultrasound services are performed exclusively for lawful medical indications. Sex determination and sex-selective practices are prohibited and punishable by law. Fetal sex is not disclosed at this centre.
Medical Disclaimer: This page is for patient education only and does not constitute medical advice. The interpretation of fetal brain findings requires expert specialist assessment — please consult Dr. Kunda Shahane for advice specific to your pregnancy.
Mayflower Fetal Medicine & High-Risk Pregnancy Centre, Dhantoli, Nagpur, provides fetal ultrasound, prenatal diagnosis, fetal echocardiography, Doppler studies, genetic counseling and high-risk pregnancy care under Dr. Kunda Shahane.

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Surdham Complex, Behind Silver Palace Building, 2nd Lane from Panchsheel Sq., Opp. Yashwant Stadium, Dhantoli Nagpur - 440012
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