Spastic Paraplegia 15, Autosomal Recessive (*)

Alternative Names

  • SPG15
  • Spastic Paraplegia and Retinal Degenration
  • Kjellin Syndrome
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WHO-ICD-10 version:2010

Diseases of the nervous system

Systemic atrophies primarily affecting the central nervous system

OMIM Number

270700

Mode of Inheritance

Autosomal recessive

Gene Map Locus

14q24.1

Epidemiology in the Arab World

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