Clinical and genetic study of a large Italian family linked to SPG12 locus

A. Orlacchio, T. Kawarai, E. Rogaeva, Y. Q. Song, A. D. Paterson, G. Bernardi, P. H. St. George-Hyslop

Research output: Contribution to journalArticle

Abstract

Background: Seven loci for autosomal dominant hereditary spastic paraplegia (ADHSP) have been mapped. To date, two families of SPG12 (chromosome 19q13) have been analyzed; however, there is not enough clinical information on SPG12 to establish locus-phenotype correlations. Methods: The authors studied 60 individuals from a large Italian family with ADHSP, in which 16 members in four generations were affected. They performed genetic linkage analysis with DNA markers from currently known ADHSP loci. After database searching, one candidate gene for SPG12 was analyzed by sequencing. Results: The patients in this family showed an early onset and rapid progression of symptoms, resulting in severe disability, with a large proportion of affected members requiring use of a wheelchair. By age 16, most patients had sensory disturbance. Evidence for linkage to the SPG12 locus was obtained. Obligate recombination events observed in this family have narrowed the SPG12 locus from the 16.1 cM to 11.3 cM region between markers D19S416 and D19S412. In combination with previous genetic studies, the SPG12 locus was further narrowed to the 3.3 cM region between D19S416 and D19S220. A homologue of the AAA (ATPases associated with a variety of cellular activities) protein family, proteasome 26S subunit ATPase mapped near D19S220, was excluded by sequencing. Conclusions: This study refined the SPG12 region between D19S416 and D19S220 and revealed several clinical characteristics - early onset, rapid progression, and involvement of sensory disturbance - that may be unique to SPG12. Suggestive evidence of genetic anticipation was obtained, but should be confirmed in other SPG12 families.

Original languageEnglish
Pages (from-to)1395-1401
Number of pages7
JournalNeurology
Volume59
Issue number9
Publication statusPublished - Nov 12 2002

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Hereditary Spastic Paraplegia
Adenosine Triphosphatases
Genetic Anticipation
Wheelchairs
Genetic Linkage
Genetic Markers
Genetic Recombination
Chromosomes
Clinical Studies
Databases
Phenotype
Genes
Proteins

ASJC Scopus subject areas

  • Neuroscience(all)

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Orlacchio, A., Kawarai, T., Rogaeva, E., Song, Y. Q., Paterson, A. D., Bernardi, G., & St. George-Hyslop, P. H. (2002). Clinical and genetic study of a large Italian family linked to SPG12 locus. Neurology, 59(9), 1395-1401.

Clinical and genetic study of a large Italian family linked to SPG12 locus. / Orlacchio, A.; Kawarai, T.; Rogaeva, E.; Song, Y. Q.; Paterson, A. D.; Bernardi, G.; St. George-Hyslop, P. H.

In: Neurology, Vol. 59, No. 9, 12.11.2002, p. 1395-1401.

Research output: Contribution to journalArticle

Orlacchio, A, Kawarai, T, Rogaeva, E, Song, YQ, Paterson, AD, Bernardi, G & St. George-Hyslop, PH 2002, 'Clinical and genetic study of a large Italian family linked to SPG12 locus', Neurology, vol. 59, no. 9, pp. 1395-1401.
Orlacchio A, Kawarai T, Rogaeva E, Song YQ, Paterson AD, Bernardi G et al. Clinical and genetic study of a large Italian family linked to SPG12 locus. Neurology. 2002 Nov 12;59(9):1395-1401.
Orlacchio, A. ; Kawarai, T. ; Rogaeva, E. ; Song, Y. Q. ; Paterson, A. D. ; Bernardi, G. ; St. George-Hyslop, P. H. / Clinical and genetic study of a large Italian family linked to SPG12 locus. In: Neurology. 2002 ; Vol. 59, No. 9. pp. 1395-1401.
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AU - Orlacchio, A.

AU - Kawarai, T.

AU - Rogaeva, E.

AU - Song, Y. Q.

AU - Paterson, A. D.

AU - Bernardi, G.

AU - St. George-Hyslop, P. H.

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N2 - Background: Seven loci for autosomal dominant hereditary spastic paraplegia (ADHSP) have been mapped. To date, two families of SPG12 (chromosome 19q13) have been analyzed; however, there is not enough clinical information on SPG12 to establish locus-phenotype correlations. Methods: The authors studied 60 individuals from a large Italian family with ADHSP, in which 16 members in four generations were affected. They performed genetic linkage analysis with DNA markers from currently known ADHSP loci. After database searching, one candidate gene for SPG12 was analyzed by sequencing. Results: The patients in this family showed an early onset and rapid progression of symptoms, resulting in severe disability, with a large proportion of affected members requiring use of a wheelchair. By age 16, most patients had sensory disturbance. Evidence for linkage to the SPG12 locus was obtained. Obligate recombination events observed in this family have narrowed the SPG12 locus from the 16.1 cM to 11.3 cM region between markers D19S416 and D19S412. In combination with previous genetic studies, the SPG12 locus was further narrowed to the 3.3 cM region between D19S416 and D19S220. A homologue of the AAA (ATPases associated with a variety of cellular activities) protein family, proteasome 26S subunit ATPase mapped near D19S220, was excluded by sequencing. Conclusions: This study refined the SPG12 region between D19S416 and D19S220 and revealed several clinical characteristics - early onset, rapid progression, and involvement of sensory disturbance - that may be unique to SPG12. Suggestive evidence of genetic anticipation was obtained, but should be confirmed in other SPG12 families.

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