Krabbe disease (globoid cell leukodystrophy) is an inherited recessive autosomal leukodystrophy caused by deficiency of the enzyme galactocerebrosidase. The lack of this enzyme leads to the build-up of galactolipids that will promote the death of oligodendrocytes and the demyelination of the central and peripheral nervous systems. There are two clinical forms: early onset and late onset. This article reports a case of late onset Krabbe disease and discusses the importance of early diagnosis for its prognosis.
CITATION STYLE
Sano, T. S. (2012). Krabbe disease: the importance of early diagnosis for prognosis. Einstein (São Paulo, Brazil), 10(2), 233–235. https://doi.org/10.1590/S1679-45082012000200019
Mendeley helps you to discover research relevant for your work.