Neuronal ceroid lipofuscinosis (NCL): classification by onset age

Evidence-based neurology checklist on neuronal ceroid lipofuscinosis (ncl): classification by onset age: NCL classification by onset age Congenital (CNCL): CLN10 Infantile (INCL): CLN1 and CLN14 Late-infantile (LICNL): CLN2 Variant infantile (VLINCL): CLN5, CLN6, CLN7, and CLN8 Juvenile (JNCL):…

NCL classification by onset age

  • Congenital (CNCL): CLN10
  • Infantile (INCL): CLN1 and CLN14
  • Late-infantile (LICNL): CLN2
  • Variant infantile (VLINCL): CLN5, CLN6, CLN7, and CLN8
  • Juvenile (JNCL): CLN3, CLN8, and CLN9
  • Adult (ACNL): CLN4, CLN12, and CLN13

References

  1. Nita DA, Mole SE, Minassian BA. Neuronal ceroid lipofuscinoses. Epileptic Disord 2016; 18:73-88. 
  2. Kousi M, Siintola E, Dvorakova L, et al. Mutations in CLN7/MFSD8 are a common cause of variant late-infantile neuronal ceroid lipofuscinosis. Brain 2009; 132:810-819.

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