Multigeneration family with dominant SPG30 hereditary spastic paraplegia

Ricardo H. Roda, Alice B. Schindler, Craig Blackstone

Research output: Contribution to journalArticle

Abstract

Autosomal recessive KIF1A missense mutations cause hereditary spastic paraplegia (HSP) type SPG30, while recessive truncations lead to sensory and autonomic neuropathy (HSN2C) and many de novo missense mutations are associated with cognitive impairment. Here, we describe family members across three generations with pure HSP. A heterozygous p.Ser69Leu KIF1A mutation segregates with those afflicted. The same variant was previously reported in a Finnish father and son with pure HSP as well as four members of a Sicilian kindred with more intrafamilial phenotypic variability. This further validates the pathogenicity of the p.Ser69Leu mutation and suggests that it may represent a mutation hot spot.

Original languageEnglish (US)
Pages (from-to)821-824
Number of pages4
JournalAnnals of Clinical and Translational Neurology
Volume4
Issue number11
DOIs
StatePublished - Nov 2017

ASJC Scopus subject areas

  • Neuroscience(all)
  • Clinical Neurology

Fingerprint Dive into the research topics of 'Multigeneration family with dominant SPG30 hereditary spastic paraplegia'. Together they form a unique fingerprint.

  • Cite this