Literature DB >> 25537619

Electrophysiological characterization of adult-onset Niemann-Pick type C disease.

Rosa Iodice1, Raffaele Dubbioso2, Antonietta Topa2, Lucia Ruggiero2, Chiara Pisciotta2, Marcello Esposito2, Stefano Tozza2, Lucio Santoro2, Fiore Manganelli2.   

Abstract

In infantile and juvenile Niemann-Pick type C (NPC) disease electrophysiological studies have shown central (CNS) and peripheral (PNS) nervous system abnormalities. However, an extensive electrophysiological evaluation of CNS and PNS in adult form of NPC is still lacking. The aim of the study is to assess in adult-onset NPC disease the involvement of CNS and PNS by a multimodal electrophysiological approach. Three patients affected by adult form of NPC disease underwent electrophysiological evaluation including nerve conduction study (NCS), magnetic motor (MEPs), visual (VEPs), somatosensory (SSEPs) and brainstem auditory (BAEPs) evoked potentials. NCS, MEPs, VEPs and upper limb SSEPs were normal. Lower limb SSEPs were abnormal in all patients and abnormalities were consistent with a length-dependent process affecting the central somatosensory pathway. BAEPs were abnormal in all patients with both peripheral and central impairment of auditory pathway. Our electrophysiological findings suggest that auditory and lower limb somatosensory pathways are constantly affected in adult-onset form of NPC disease. The involvement of PNS, pyramidal, visual and upper limb somatosensory pathways might occur later during the course of disease.
Copyright © 2014 Elsevier B.V. All rights reserved.

Entities:  

Keywords:  Auditory pathway; Brainstem pathology; Length dependent axonopathy; Multimodal evoked potential; Niemann–Pick disease type C; Somatosensory pathway

Mesh:

Year:  2014        PMID: 25537619     DOI: 10.1016/j.jns.2014.12.005

Source DB:  PubMed          Journal:  J Neurol Sci        ISSN: 0022-510X            Impact factor:   3.181


  11 in total

1.  Pseudo-orthostatic tremor: description of a not typical case.

Authors:  Aniello Iovino; Silvio Peluso; Fiore Manganelli; Stefano Tozza; Marcello Esposito
Journal:  Neurol Sci       Date:  2019-06-12       Impact factor: 3.307

2.  Different cortical excitability profiles in hereditary brain iron and copper accumulation.

Authors:  Raffaele Dubbioso; Lucia Ruggiero; Marcello Esposito; Paola Tarantino; Marcello De Angelis; Francesco Aruta; Sabina Pappatà; Lorenzo Ugga; Alberto Piperno; Raffaele Iorio; Lucio Santoro; Rosa Iodice; Fiore Manganelli
Journal:  Neurol Sci       Date:  2019-11-26       Impact factor: 3.307

3.  Long-term therapy with miglustat and cognitive decline in the adult form of Niemann-Pick disease type C: a case report.

Authors:  Stefano Tozza; Raffaele Dubbioso; Rosa Iodice; Antonietta Topa; Marcello Esposito; Lucia Ruggiero; Emanuele Spina; Anna De Rosa; Francesco Saccà; Lucio Santoro; Fiore Manganelli
Journal:  Neurol Sci       Date:  2018-03-13       Impact factor: 3.307

Review 4.  Recent neuroimaging, neurophysiological, and neuropathological advances for the understanding of NPC.

Authors:  Alberto Benussi; Maria Sofia Cotelli; Alessandro Padovani; Barbara Borroni
Journal:  F1000Res       Date:  2018-02-15

5.  Facioscapulohumeral muscular dystrophy (FSHD) and multiple sclerosis: a case report.

Authors:  Rosa Iodice; Lorenzo Ugga; Francesco Aruta; Aniello Iovino; Lucia Ruggiero
Journal:  Acta Myol       Date:  2020-03-01

6.  In vivo evidence of cortical amyloid deposition in the adult form of Niemann Pick type C.

Authors:  Marcello Esposito; Raffaele Dubbioso; Stefano Tozza; Rosa Iodice; Marco Aiello; Emanuele Nicolai; Carlo Cavaliere; Marco Salvatore; Lucio Santoro; Fiore Manganelli
Journal:  Heliyon       Date:  2019-11-14

7.  Peripheral neuropathy as a very rare symptom in a patient with Niemann-Pick type C with negative enzymatic evaluation: a case report.

Authors:  Mohammad Barzegar; Fatemeh Valaee; Shadi Ghoreishizadeh
Journal:  J Med Case Rep       Date:  2022-01-12

8.  Visual evoked potentials of Niemann-Pick type C1 mice reveal an impairment of the visual pathway that is rescued by 2-hydroxypropyl-ß-cyclodextrin.

Authors:  Giampiero Palladino; Stefano Loizzo; Andrea Fortuna; Sonia Canterini; Fioretta Palombi; Robert P Erickson; Franco Mangia; Maria Teresa Fiorenza
Journal:  Orphanet J Rare Dis       Date:  2015-10-12       Impact factor: 4.123

9.  Adult Niemann-Pick disease type C in France: clinical phenotypes and long-term miglustat treatment effect.

Authors:  Yann Nadjar; Ana Lucia Hütter-Moncada; Philippe Latour; Xavier Ayrignac; Elsa Kaphan; Christine Tranchant; Pascal Cintas; Adrian Degardin; Cyril Goizet; Chloe Laurencin; Lionel Martzolff; Caroline Tilikete; Mathieu Anheim; Bertrand Audoin; Vincent Deramecourt; Thierry Dubard De Gaillarbois; Emmanuel Roze; Foudil Lamari; Marie T Vanier; Bénédicte Héron
Journal:  Orphanet J Rare Dis       Date:  2018-10-01       Impact factor: 4.123

Review 10.  Current Challenges in Understanding the Cellular and Molecular Mechanisms in Niemann-Pick Disease Type C1.

Authors:  Anja U Bräuer; Angela Kuhla; Carsten Holzmann; Andreas Wree; Martin Witt
Journal:  Int J Mol Sci       Date:  2019-09-06       Impact factor: 5.923

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