• Neel H Mehta, Eduardo A Maury, Zachary Buller, Phan Q Duy, Carla Fortes, Seth L Alper, E Zeynep Erson-Omay, and Kristopher T Kahle.
• 1Department of Neurosurgery, Harvard Medical School and Massachusetts General Hospital, Boston, Massachusetts.
• J. Neurosurg. 2024 Aug 23: 171-7.

AbstractIdiopathic normal pressure hydrocephalus (iNPH) is characterized by dilation of the cerebral ventricles without increased cerebral pressure. Patients typically present with cognitive impairment, gait abnormalities, and urinary incontinence. Despite current guidelines for diagnosis and surgical intervention, there is little consensus on the pathophysiology of iNPH. Familial cases and genomic studies of iNPH have recently suggested an underappreciated role of genetics in disease pathogenesis, implicating mechanisms ranging from dysregulated CSF dynamics to underlying neurodegenerative or neuroinflammatory processes. In this paper, the authors provide a brief review of genetic insights and candidate genes for iNPH, highlighting the continued importance of integrated genetic analysis and clinical studies to advance iNPH management.

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