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Imaging in atypical van der knaap disease with subependymal nodular heterotopia: A case report
Pramod V1, Sanjay S C2, Dheepika R3
1Senior Resident, Department of Radiodiagnosis, Kempegowda Institute of Medical Sciences Hospital and Research Centre, Rajiv Gandhi University of Health Sciences, Bangalore, 560004, Karnataka, India.
Abstract:
Here, we discuss a rare and to our knowledge, the first case of an atypical Van der Knaap's disease in a 6-year-old boy who presented with motor difficulties, developmental delay, cognitive impairment, seizures. The objective of this report is to highlight its unusual findings on MRI including internal capsule, brainstem, cerebellum involvement; subependymal nodular heterotopia, subependymal cysts, cortical laminar necrosis along with typical findings of megalencephalic leukoencephalopathy and subcortical cysts. The study also underscores the clinical implications of this complex pathology, with emphasis on comprehensive neuroradiological evaluation for atypical presentations to guide better diagnostic and management outcomes.
Insights
This report details the first known atypical Van der Knaap
Area of Science:
- Neurology
- Radiology
- Genetics
Background:
- Van der Knaap's disease is a rare genetic leukoencephalopathy.
- Atypical presentations can pose diagnostic challenges.
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