# Clinical Profile, Magnetic Resonance Imaging (MRI) Findings, and Neurological Outcomes in Neonatal Rotavirus Encephalitis: A Prospective Observational Study

**Authors:** Vikram Sakaleshpur Kumar, Prashanth S Veeraiah, Gifty Mathew

PMC · DOI: 10.7759/cureus.100232 · 2025-12-28

## TL;DR

This study examines neonatal rotavirus encephalitis, finding that MRI patterns predict long-term neurological outcomes.

## Contribution

The study provides new clinical and MRI data on neonatal rotavirus encephalitis and its developmental consequences.

## Key findings

- MRI abnormalities in neonatal rotavirus encephalitis strongly predict adverse neurodevelopmental outcomes.
- Early-onset seizures and specific MRI signatures are key indicators of neurological impairment in affected neonates.

## Abstract

Background: Rotavirus, classically an enteric pathogen, is now recognized as a neurotropic virus capable of causing neonatal encephalitis. Its neurological effects, though rare, have significant developmental consequences.

Objective: This study aimed to evaluate the clinical profile, magnetic resonance imaging (MRI) findings, and neurological outcomes in neonates with rotavirus encephalitis.

Methods: A prospective observational study was conducted in the Neonatal Intensive Care Unit of Sarji Maternal and Child Hospital, Shivamogga, India, from April 2023 to March 2025. Twenty-five neonates aged three to nine days presenting with seizures and encephalopathy were included if MRI suggested viral encephalitis and stool reverse transcriptase polymerase chain reaction (RT-PCR) was positive for rotavirus. Demographic, clinical, biochemical, and radiologic data were prospectively recorded and analyzed using Statistical Package for the Social Sciences version 24 (IBM Corp., Armonk, NY).

Results: Among 25 neonates, 13 (52%) were female and 12 (48%) were male neonates; 20 (80%) were term, and five (20%) were preterm. Nineteen (76%) were outborn, and six (24%) were inborn. Seizure onset occurred less than or equal to four days in 11 (44 %), on day 5 in eight (32%), and after day 5 in six (24%). Common accompanying symptoms were lethargy/poor feeding in 13 (52%), diarrhea or vomiting in eight (32%), and respiratory distress in five (20%). Laboratory findings showed leukocytosis in 15 (60%), thrombocytopenia in 10 (40%), hypocalcemia in five (20%), C-reactive protein positivity in seven (28%), CSF pleocytosis in 12 (48%), and protein elevation in 14 (56%). All 23 tested (100%) had stool RT-PCR-positive for rotavirus. MRI revealed symmetric periventricular±basal ganglia involvement in 14 (56%), superficial periventricular white-matter lesions in eight (32%), and extensive periventricular+deep-gray±brainstem lesions in three (12%). At discharge, 17 (68%) had hypertonia, three (12%) hypotonia, and five (20%) normal tone. At the one-year follow-up, 15 (60%) had normal development, whereas 10 (40%) had abnormal outcomes: global developmental delay in seven (28%), postencephalitic epilepsy in two (8%), and spastic cerebral palsy in one (4%). The severity of MRI abnormalities was strongly associated with adverse neurodevelopmental outcomes (p < 0.001).

Conclusion: Neonatal rotavirus encephalitis manifests with early-onset seizures and distinct MRI signatures that predict later neurological impairment. Early MRI evaluation and structured long-term developmental surveillance are crucial to improving outcomes.

## Linked entities

- **Diseases:** spastic cerebral palsy (MONDO:0000396)
- **Species:** Homo sapiens (taxon 9606)

## Full-text entities

- **Genes:** CRP (C-reactive protein) [NCBI Gene 1401] {aka PTX1}
- **Diseases:** leukocytosis (MESH:D007964), hypocalcemia (MESH:D006996), Rotavirus Encephalitis (MESH:D012400), brainstem lesions (MESH:D020295), spastic cerebral palsy (MESH:D002547), hypertonia (MESH:D009122), vomiting (MESH:D014839), neurological impairment (MESH:D009422), Seizure (MESH:D012640), thrombocytopenia (MESH:D013921), white-matter lesions (MESH:D056784), developmental delay (MESH:D002658), viral encephalitis (MESH:D018792), neonatal encephalitis (MESH:D004660), lethargy (MESH:D053609), hypotonia (MESH:D009123), enteric pathogen (MESH:D004751), encephalopathy (MESH:D001927), respiratory distress (MESH:D012128), postencephalitic epilepsy (MESH:D010301), diarrhea (MESH:D003967)
- **Species:** Rotavirus (genus) [taxon 10912]

## Figures

1 figure with captions in the complete paper: https://tomesphere.com/paper/PMC12835956/full.md

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Source: https://tomesphere.com/paper/PMC12835956