Spastic paraplegia, optic atrophy, and neuropathy is linked to chromosome 11q13

Ann Neurol. 2005 May;57(5):730-7. doi: 10.1002/ana.20478.

Abstract

We report an autosomal recessive neurodegenerative disorder in 25 white members from a large inbred Brazilian family, 22 of whom were evaluated clinically. This condition is characterized by (1) subnormal vision secondary to apparently nonprogressive congenital optic atrophy; (2) onset of progressive spastic paraplegia in infancy; (3) onset of progressive motor and sensory axonal neuropathy in late childhood/early adolescence; (4) dysarthria starting in the third decade of life; (5) exacerbated acoustic startle response; and (6) progressive joint contractures and spine deformities. Motor handicap was severe, and all patients were wheelchair bound after 15 years old. We performed a genome-wide screen including 25 affected individuals and 49 of their unaffected relatives. Linkage was detected at 11q13 region with a maximum logarithm of odds score of +14.43, obtained with marker D11S1883. The candidate region, which lies between D11S1908 and D11S1889, encompasses approximately 4.8Mb and has more than 100 genes and expressed sequences. We propose the acronym SPOAN (spastic paraplegia, optic atrophy, and neuropathy) for this complex syndrome.

Publication types

  • Case Reports
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Abnormalities, Multiple / genetics
  • Adolescent
  • Adult
  • Age of Onset
  • Brazil
  • Child
  • Chromosome Mapping
  • Chromosomes, Human, Pair 11 / genetics*
  • DNA / genetics
  • Disease Progression
  • Dysarthria / genetics
  • Female
  • Genetic Linkage / genetics
  • Hereditary Sensory and Motor Neuropathy / genetics*
  • Humans
  • Joints / abnormalities
  • Male
  • Microsatellite Repeats
  • Middle Aged
  • Optic Atrophies, Hereditary / genetics*
  • Paraplegia / genetics*
  • Pedigree
  • Reflex, Startle / physiology
  • Spine / abnormalities

Substances

  • DNA