Cited by 39

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Pure adult-onset Spastic Paraplegia caused by a novel mutation in the KIAA0196 (SPG8) gene

Bot, Susanne T., Vermeer, Sascha, Buijsman, Wendy, Heister, Angelien, Voorendt, Marsha, Verrips, Aad, Scheffer, Hans, Kremer, Hubertus P. H., Warrenburg, Bart P. C., Kamsteeg, Erik-Jan·2013·Journal of Neurology

Abstract

SPG8 is a rare autosomal dominant hereditary spastic paraplegia (AD-HSP), with only six SPG8 families described so far. Our purpose was to screen for KIAA0196 (SPG8) mutations in AD-HSP patients and to investigate their phenotype. Extensive family investigation was performed after positive KIAA0196 mutation analysis, which was part of an on-going mutation screening effort in AD-HSP patients. A novel pathogenic KIAA0196 mutation p.(Gly696Ala) was identified in two AD-HSP patients, who subsequently were shown to belong to a single large Dutch pedigree with more than 10 affected family members. The phenotype consisted of a pure HSP with ages at onset between 20 and 60 years, distally reduced vibration sense in the legs in all, and urinary urgency in seven out of 10 patients. Frequent features were exercise- or emotion-induced increase of spasticity and gait problems and chronic nonspecific lower back and joint pains. We have identified a fourth pathogenic KIAA0196 mutation in a Dutch HSP-family, the seventh family worldwide, with a less severe clinical course than described before.

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Crossref · 10.1007/s00415-013-6870-x

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  • SPG8 is a rare autosomal dominant HSP characterized by onset of progressive lower limb spasticity and hyperreflexia in adults, resulting in impaired gait and difficulty in walking.

    “SPG8 is a rare autosomal dominant HSP characterized by onset of progressive lower limb spasticity and hyperreflexia in adults, resulting in impaired gait and difficulty in walking.”

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Research works printed but not linked: 12

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  2. Derivery E, Sousa C, Gautier JJ, Lombard B, Loew D, Gautreau A (2009) The Arp2/3 activator WASH controls the fission of endosomes through a large multiprotein complex. Dev Cell 17:712–723 · DOI · Paper page
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  4. de Bot ST, Schelhaas HJ, Kamsteeg EJ, van de Warrenburg BP (2012) Hereditary spastic paraplegia caused by a mutation in the VCP gene. Brain 135:e223 · DOI
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  8. Venselaar H, Te Beek TA, Kuipers RK, Hekkelman ML, Vriend G (2010) Protein structure analysis of mutations causing inheritable diseases. An e-Science approach with life scientist friendly interfaces. BMC Bioinformatics 11:548 · DOI
  9. Moller P, Clark N, Maehle L (2011) A SImplified method for Segregation Analysis (SISA) to determine penetrance and expression of a genetic variant in a family. Hum Mutat 32:568–571 · DOI
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  11. Reid E, Dearlove AM, Whiteford ML, Rhodes M, Rubinsztein DC (1999) Autosomal dominant spastic paraplegia: refined SPG8 locus and additional genetic heterogeneity. Neurology 53:1844–1849 · DOI
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Metadata

Authors
Bot, S. T., Vermeer, S., Buijsman, W., Heister, A., Voorendt, M., Verrips, A., Scheffer, H., Kremer, H. P. H., Warrenburg, B. P. C., & Kamsteeg, E.-J.
Venue
Journal of Neurology
Published
2013-03-02
Volume
260
Issue
7
Pages
1765-1769
ISSN
  • 0340-5354
  • 1432-1459
Cited by
39
References
0
Language
en

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