Article
[Mucopolysaccharidosis type I in the Cuban population].
Revista de neurologia - 1 Jan 2000
Menéndez-Sainz C, Zaldívar-Muñoz C, González-Quevedo A
Abstract excerpt
INTRODUCTION: Of all the innate errors of the metabolism, the mucopolysaccharidoses (MPS), a kind of lysosomal disease, are especially significant because of the serious clinical features they give rise to and the therapeutic difficulties they entail. Diagnosis of the index case is essential so that families can gain access to the preventive benefits of genetic counselling. To date, seven types of MPS and 11...
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