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  • Kamm, C (author)

The fragile X tremor ataxia syndrome in the differential diagnosis of multiple system atrophy: data from the EMSA Study Group

  • Article/chapterEnglish2005

Publisher, publication year, extent ...

  • 2005-06-09
  • Oxford University Press (OUP),2005

Numbers

  • LIBRIS-ID:oai:lup.lub.lu.se:dc3554eb-3b1a-4646-bc1e-670f9ed1d314
  • https://lup.lub.lu.se/record/232158URI
  • https://doi.org/10.1093/brain/awh535DOI

Supplementary language notes

  • Language:English
  • Summary in:English

Part of subdatabase

Classification

  • Subject category:art swepub-publicationtype
  • Subject category:ref swepub-contenttype

Notes

  • The recent identification of fragile X-associated tremor ataxia syndrome (FXTAS) associated with premutations in the FMR1 gene and the possibility of clinical overlap with multiple system atrophy (MSA) has raised important questions, such as whether genetic testing for FXTAS should be performed routinely in MSA and whether positive cases might affect the specificity of current MSA diagnostic criteria. We genotyped 507 patients with clinically diagnosed or pathologically proven MSA for FMR1 repeat length. Among the 426 clinically diagnosed cases, we identified four patients carrying FMR1 premutations (0.94%). Within the subgroup of patients with probable MSA-C, three of 76 patients (3.95%) carried premutations. We identified no premutation carriers among 81 patients with pathologically proven MSA and only one carrier among 622 controls (0.16%). Our results suggest that, with proper application of current diagnostic criteria, FXTAS is very unlikely to be confused with MSA. However, slowly progressive disease or predominant tremor are useful red flags and should prompt the consideration of FXTAS. On the basis of our data, the EMSA Study Group does not recommend routine FMR1 genotyping in typical MSA patients.

Subject headings and genre

Added entries (persons, corporate bodies, meetings, titles ...)

  • Healy, DG (author)
  • Quinn, NP (author)
  • Wullner, U (author)
  • Moller, JC (author)
  • Schols, L (author)
  • Geser, F (author)
  • Burk, K (author)
  • Borglum, AD (author)
  • Pellecchia, MT (author)
  • Tolosa, E (author)
  • del Sorbo, F (author)
  • Nilsson, ChristerLund University,Lunds universitet,Psykiatri, Lund,Sektion IV,Institutionen för kliniska vetenskaper, Lund,Medicinska fakulteten,Psychiatry (Lund),Section IV,Department of Clinical Sciences, Lund,Faculty of Medicine(Swepub:lu)neur-cni (author)
  • Bandmann, O (author)
  • Sharma, M (author)
  • Mayer, P (author)
  • Gasteiger, M (author)
  • Haworth, A (author)
  • Ozawa, T (author)
  • Lees, AJ (author)
  • Short, J (author)
  • Giunti, P (author)
  • Holinski-Feder, E (author)
  • Illig, T (author)
  • Wichmann, HE (author)
  • Wenning, GK (author)
  • Wood, NW (author)
  • Gasser, T (author)
  • Psykiatri, LundSektion IV (creator_code:org_t)

Related titles

  • In:Brain: Oxford University Press (OUP)128:8, s. 1855-18601460-21560006-8950

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