A novel locus for an autosomal recessive hereditary spastic paraplegia (SPG35) maps to 16q21-q23

K. J. Dick, R. Al-Mjeni, W. Baskir, R. Koul, M. A. Simpson, M. A. Patton, S. Raeburn, A. H. Crosby

Research output: Contribution to journalArticlepeer-review

46 Citations (Scopus)


Background: The hereditary spastic paraplegias (HSPs) are a group of clinically and genetically heterogeneous neurodegenerative disorders in which the cardinal pathologic feature is upper motor neuron degeneration leading to progressive spasticity and weakness of the lower limbs. To date, 14 autosomal recessive HSP loci have been mapped. Methods: We have identified a large consanguineous Omani family in which an autosomal recessive form of HSP is segregating. The age at onset varied from 6 to 11 years and the course of the disease is progressive with intellectual disability and is associated with seizures in two individuals. To map the chromosomal location of the causative gene we undertook 250K gene chip SNP analyses of all affected individuals assuming that a founder mutation was responsible. Results: All affected individuals shared a 20.4 Mb (3.25 cM) region of homozygosity located on chromosome 16q21-q23.1, defined by SNP markers rs149428 and rs9929635 (peak multipoint lod score of 4.86). Two candidate genes, dynein, cytoplasmic 1, light intermediate chain 2 (DYNC1LI2) and vacuolar protein sorting 4 homolog A (VPS4A), were sequenced but no disease causing mutations were identified. Conclusion: We have mapped the chromosomal location of a novel gene responsible for a form of hereditary spastic paraplegia (HSP) (SPG35) and defined its clinical presentation.

Original languageEnglish
Pages (from-to)248-252
Number of pages5
Issue number4
Publication statusPublished - Jul 22 2008

ASJC Scopus subject areas

  • Clinical Neurology


Dive into the research topics of 'A novel locus for an autosomal recessive hereditary spastic paraplegia (SPG35) maps to 16q21-q23'. Together they form a unique fingerprint.

Cite this