Publications by authors named "R G van Gool"

Background: Niemann-Pick Disease Type C (NPC) is an ultra-rare disorder characterized by progressive psychiatric and neurologic manifestations, with late infantile, juvenile, and adolescent/adult presentations. We examined morphological properties of the choroid plexus, a protective blood-cerebrospinal fluid barrier, in NPC, and their relationship with neurodegeneration, clinical status, and circulatory markers. This study also determined whether choroid plexus morphology differentiates between NPC and more prevalent illnesses, schizophrenia (SZ) and bipolar disorder (BD), which have overlapping psychiatric symptoms with adolescent and adult-onset NPC and are associated with misdiagnosis.

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Article Synopsis
  • Niemann-Pick disease type C (NPC) is a rare genetic disorder causing neurodegeneration and impairments in speech and cognitive functions.
  • The study assessed 8 adults with NPC and healthy controls, using various tests including brain imaging, to identify issues in motor skills, speech production, and cognitive abilities.
  • Findings showed significant brain volume and structural changes in NPC patients, linking these to their motor and cognitive deficits, and suggesting potential biomarkers for understanding the disease better.*
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The current study aims to characterize brain morphology of pain as reported by small fiber neuropathy (SFN) patients with or without a gain-of-function variant involving the SCN9A gene and compare these with findings in healthy controls without pain. The Neuropathic Pain Scale was used in patients with idiopathic SFN (N = 20) and SCN9A-associated SFN (N = 12) to capture pain phenotype. T1-weighted, structural magnetic resonance imaging (MRI) data were collected in patients and healthy controls (N = 21) to 1) compare cortical thickness and subcortical volumes and 2) quantify the association between severity, quality, and duration of pain with morphological properties.

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  • Pompe disease is a rare genetic disorder caused by a deficiency in acid alpha-glucosidase, leading to muscle weakness and other symptoms, often neglecting pain and psychological aspects.
  • A case study discusses a child with late-onset Pompe disease who experiences chronic pain, diagnosed at 9 years old after various initial misattributions.
  • Treatment includes enzyme replacement therapy and a multidisciplinary approach focusing on physical and psychosocial therapies to manage pain and improve the child's overall well-being.
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Article Synopsis
  • Niemann-Pick disease type C (NPC) is a rare genetic disorder that leads to the buildup of cholesterol and lipids in cells, causing various neurological and systemic issues, affecting both patients and their caregivers over time.
  • *Focus group discussions with 19 individuals, including both patients and caregivers, identified key concerns such as cognitive decline, motor function impairment, loss of independence, and social isolation.
  • *The feedback from these discussions also highlighted challenges related to participating in research, particularly logistical issues around travel and the need for sedation during MRI scans, while offering insights for future studies on NPC.
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