Late infantile metachromatic leucodystrophy (MLD) View Full Text


Ontology type: schema:ScholarlyArticle     


Article Info

DATE

1975-12

AUTHORS

Livia N. Rossi, Franco Vassella, Albert Bischoff, Ulrich N. Wiesmann, Norbert Herschkowitz

ABSTRACT

A typical case of late infantile MLD is presented with all available clinical, morphological and biochemical results. The diagnostical value of the different parameters is evaluated and the pathogenesis of the disorder discussed. In spite of successful experimental enzyme substitution in cultured MLD fibroblasts with restitution of function by added Arylsulfatase, the therapeutic possibilities for the fatal disease in the patients are extremely limited. More... »

PAGES

291-298

Identifiers

URI

http://scigraph.springernature.com/pub.10.1007/bf00316530

DOI

http://dx.doi.org/10.1007/bf00316530

DIMENSIONS

https://app.dimensions.ai/details/publication/pub.1044707064

PUBMED

https://www.ncbi.nlm.nih.gov/pubmed/52698


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