Article
Clinical and laboratorial study of 19 cases of mucopolysaccharidoses.
Revista do Hospital das Clinicas - 1 Jan 2000
Albano L M, Sugayama S S, Bertola D R, Andrade C E, Utagawa C Y, Puppi F, Nader H B, Toma L, Coelho J, Leistner S, Burin M, Giugliani R, Chong A K
Abstract excerpt
UNLABELLED: The mucopolysaccharidoses (MPS) are a heterogeneous group of inborn errors of lysosomal glycosaminoglycan (GAG) metabolism. The importance of this group of disorders among the inborn errors of metabolism led us to report 19 cases. METHOD: We performed clinical, radiological, and biochemical evaluations of the suspected patients, which allowed us to establish a definite diagnosis in 19 cases. RESULTS:...
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