Literature DB >> 28320130

SPG2 mimicking multiple sclerosis in a family identified using next generation sequencing.

Anna Rubegni1, Carla Battisti2, Alessandra Tessa1, Alfonso Cerase3, Stefano Doccini1, Alessandro Malandrini2, Filippo M Santorelli4, Antonio Federico5.   

Abstract

Several single gene disorders can potentially be overlooked in the differential diagnostic evaluation of patients with multiple sclerosis (MS). Pelizaeus-Merzbacher disease and spastic paraplegia type 2 are allelic X-linked disorders associated with defective myelination of the central nervous system and mutations in PLP1. Neurological symptoms are occasionally observed in female carriers of these mutations. Two women - the proposita (Pt1) and her mother (Pt2) - reported walking difficulties since adolescence and showed progressive cognitive decline. Their neurological examinations revealed spastic gait, pyramidal tract involvement and distal muscle atrophy in the legs. Peripheral neuropathy and diffuse white matter (WM) changes on brain MRI were also observed. Both patients had a preliminary diagnosis of primary progressive MS. Using a targeted method in next generation sequencing, the novel heterozygous c.210T>G/p.Y70* in PLP1 was identified in Pt2. The same mutation was also found in Pt1 but not in five healthy relatives. The mutation showed moderate-to-severe skewed X inactivation in tissues, and Western blotting revealed a significant reduction of PLP1 and DM20 in the sural nerve of Pt2. In conclusion a mother and daughter presented an X-linked dominant disorder with skewed X inactivation. The authors suggest that PLP1 testing might be considered in the evaluation of women with spastic paraparesis, cognitive decline and WM changes.
Copyright © 2017 Elsevier B.V. All rights reserved.

Entities:  

Keywords:  Hereditary spastic paraparesis; MRI; Multiple sclerosis; PLP1

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Year:  2017        PMID: 28320130     DOI: 10.1016/j.jns.2017.01.069

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


  4 in total

1.  PLP1 Mutations in Patients with Multiple Sclerosis: Identification of a New Mutation and Potential Pathogenicity of the Mutations.

Authors:  Nancy C Cloake; Jun Yan; Atefeh Aminian; Michael P Pender; Judith M Greer
Journal:  J Clin Med       Date:  2018-10-11       Impact factor: 4.241

Review 2.  Neuroimaging in Hereditary Spastic Paraplegias: Current Use and Future Perspectives.

Authors:  Felipe Franco da Graça; Thiago Junqueira Ribeiro de Rezende; Luiz Felipe Rocha Vasconcellos; José Luiz Pedroso; Orlando Graziani P Barsottini; Marcondes C França
Journal:  Front Neurol       Date:  2019-01-16       Impact factor: 4.003

Review 3.  Challenges and Controversies in the Genetic Diagnosis of Hereditary Spastic Paraplegia.

Authors:  Lydia Saputra; Kishore Raj Kumar
Journal:  Curr Neurol Neurosci Rep       Date:  2021-02-28       Impact factor: 5.081

4.  Machine-learning based lipid mediator serum concentration patterns allow identification of multiple sclerosis patients with high accuracy.

Authors:  Jörn Lötsch; Susanne Schiffmann; Katja Schmitz; Robert Brunkhorst; Florian Lerch; Nerea Ferreiros; Sabine Wicker; Irmgard Tegeder; Gerd Geisslinger; Alfred Ultsch
Journal:  Sci Rep       Date:  2018-10-05       Impact factor: 4.379

  4 in total

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