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Opercular syndrome: A case report and review.
Soaham Dilip Desai1, Dipen Patel, Sheela Bharani
1Department of Neuromedicine, Shree Krishna Hospital, Pramukhswami Medical College, Karamsad, Gujarat, India.
This case study highlights a 9-year-old boy with bilateral opercular syndrome, resulting from perinatal asphyxia. The condition caused significant speech, swallowing, and motor delays, alongside complex partial seizures.
Area of Science:
- Neurology
- Pediatrics
- Developmental Neuroscience
Background:
- Perinatal asphyxia and neonatal seizures can lead to long-term neurological deficits.
- Bilateral opercular syndrome is a rare neurological condition affecting motor control of the face, tongue, and pharynx.
Observation:
- A 9-year-old boy presented with delayed speech, motor, and mental milestones following perinatal asphyxia.
- Clinical examination revealed bilateral trigemino-facio-linguo-pharyngeal palsy affecting voluntary movements, with preserved automatic and emotional movements.
- The patient experienced dysarthria, dysphagia, drooling, and complex partial seizures.
Findings:
- Electroencephalography showed focal left fronto-temporal epileptiform discharges.
- Brain imaging indicated bilateral cortical and subcortical encephalomalacia, predominantly in the opercular regions.
- The clinical and neuroimaging findings were consistent with bilateral opercular syndrome.
Implications:
- This case underscores the potential for perinatal insults to cause severe developmental and neurological impairments.
- Early identification and management of symptoms associated with bilateral opercular syndrome are crucial for affected children.
- Further research into the long-term outcomes and therapeutic strategies for bilateral opercular syndrome is warranted.
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