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Cerebral lipidoses

Metabolic Diseases

by Alexander Kurz

This chapter summarises a group of diseases caused by enzyme defects, which result in the accumulation of abnormal lipid materials. The enzyme defects are due to mutations with autosomal recessive inheritance. Usually, these storage diseases have an onset at an infantile or juvenile age, but there are rare variants with adult onset.

 

 
 

Last Updated: vendredi 09 octobre 2009

 

 
  • Acknowledgements

    This information was gathered in the framework of the European Commission financed project "Rare forms of dementia". Neither the European Commission nor any person acting on its behalf is responsible for any use that might be made of the following information.
  • European Union
 
 

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