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April 3, 2026Movement Disorders Clinical Practice0 citations

Niemann Pick Type C Presenting as Familial Late‐Onset Richardson Syndrome. A Case Series of Four Siblings

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VCVasilios ConstantinidesCKChristos KorosAKAndreas Kyrozis

Key Points

  • To investigate the presentation of late-onset Niemann Pick Type C (NP-C) in four siblings and its mimicry of Richardson syndrome.
  • Case series of four siblings with late-onset NP-C symptoms
  • Genetic analysis for NPC-1 gene mutations
  • Clinical evaluation of Richardson syndrome characteristics
  • All four siblings exhibit late-onset symptoms similar to Richardson syndrome
  • Identified the c.2861C>T mutation in the NPC-1 gene in each case
  • Symptoms included motor dysfunction and cognitive decline

Abstract

Late onset (>40 years) NP-C, particularly due to c.2861C>T, p.(Ser954Leu) mutation in the NPC-1 gene, can mimic Richardson syndrome.

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Cite This Study

Constantinides et al. (2026) studied this question.

synapsesocial.com/papers/69cf5dd55a333a821460bd3fhttps://doi.org/10.1002/mdc3.70613
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Also Consider

Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context:

  1. 1Clinical Aspects of Niemann-Pick Type C Disease in the Adult1991 · 41 citations
  2. 2EEG findings in early-stage corticobasal degeneration and progressive supranuclear palsy: A retrospective study and literature review2006 · 22 citations
  3. 3Prevalence of Lysosomal Storage Disorders1999 · 2,212 citations
  4. 4Audiologic Profile in Niemann‐Pick C1991 · 16 citations
  5. 5Two Patients with Niemann Pick Disease Type C Diagnosed in the Seventh Decade of Life2020 · 8 citations