Metachromatic leukodystrophy - Mutation analysis provides further evidence of genotype-phenotype correlation

Alessandra Biffi, M. Cesani, F. Fumagalli, U. Del Carro, C. Baldoli, S. Canale, S. Gerevini, S. Amadio, M. Falautano, A. Rovelli, G. Comi, M. G. Roncarolo, Maria Sessa

Research output: Contribution to journalArticlepeer-review


Metachromatic leukodystrophy (MLD) is a rare lysosomal storage disorder resulting from the inherited deficiency of the arylsulfatase A (ARSA) enzyme. Currently, no valid therapeutic options are available for affected patients. A thorough knowledge of disease progression in its diverse clinical variants, together with the identification of reliable prognostic factors, could be instrumental in accurate patient selection for new upcoming therapeutic opportunities, such as enzyme replacement and gene therapy. The described correlation between genotype and clinical presentation proved helpful in predicting patient's prognosis, only in the minority of MLD patients harboring common mutations. Molecular characterization of a cohort of 26 MLD patients allowed us to identify 18 mutations, excluding the common 0 and R alleles, 10 of which are rare and 8 are novel. By categorizing the rare mutations, we were able to confirm a correlation between ARSA gene mutations, age at onset and patterns of disease progression, not only in those patients bearing common mutations, but also in those carrying rare mutant alleles. Moreover, in the case of absent or delayed molecular diagnosis, or of newly identified mutations, the involvement of peripheral nervous system from disease onset proved to be a sensitive prognostic marker predicting a severe progression.

Original languageEnglish
Pages (from-to)349-357
Number of pages9
JournalClinical Genetics
Issue number4
Publication statusPublished - 2008


  • Genotype
  • Metachromatic leukodystrophy
  • Natural history
  • Peripheral nervous system
  • Phenotype
  • Rare mutations

ASJC Scopus subject areas

  • Genetics(clinical)
  • Genetics


Dive into the research topics of 'Metachromatic leukodystrophy - Mutation analysis provides further evidence of genotype-phenotype correlation'. Together they form a unique fingerprint.

Cite this