Cognitive dysfunction and psychosis: expanding the phenotype of SPG7

Neurocase. 2021 Jun;27(3):253-258. doi: 10.1080/13554794.2021.1927114. Epub 2021 May 18.

Abstract

Spastic paraplegia type 7 (SPG7) is one of the most common forms of autosomal recessive hereditary spastic paraplegia, which can lead to a hybrid spastic-ataxic phenotype. Recently, novel complicated forms of SPG7, including cognitive and social impairment phenotypes, have been reported. We present a SPG7 case with two pathogenic variants in compound heterozygosity in the SPG7 gene, featuring a cerebellar cognitive affective syndrome with psychosis not yet described in the literature.

Keywords: Hereditary spastic paraplegia; SPG7; cerebellar cognitive affective syndrome; cognition; psychosis.

Publication types

  • Case Reports

MeSH terms

  • ATPases Associated with Diverse Cellular Activities / genetics
  • Cognitive Dysfunction* / genetics
  • Humans
  • Metalloendopeptidases / genetics
  • Mutation
  • Phenotype
  • Psychotic Disorders* / complications
  • Psychotic Disorders* / genetics

Substances

  • Metalloendopeptidases
  • SPG7 protein, human
  • ATPases Associated with Diverse Cellular Activities