Management of mucopolysaccharidosis type VI in adults

Mucopolysaccharidosis type VI (Maroteaux-Lamy syndrome, MPS VI) is a progressive multisystemic lysosomal storage disease. Physical symptoms generally include growth retardation, and bone dysplasia. Enzyme replacement therapy is the treatment of choice and is done with recombinant version of enzyme N...

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Veröffentlicht in:	Liječnički vjesnik 2015-07, Vol.137 (7-8), p.213-215
Hauptverfasser:	Muačević-Kataneć, Diana, Pećin, Ivan, Šimić, Iveta, Fumić, Ksenija, Potočki, Kristina, Šućur, Nediljko, Reiner, Željko
Format:	Artikel
Sprache:	hrv
Schlagworte:	Adult Croatia Enzyme Replacement Therapy Humans Mucopolysaccharidosis VI - diagnosis Mucopolysaccharidosis VI - therapy N-Acetylgalactosamine-4-Sulfatase - therapeutic use Recombinant Proteins - therapeutic use
Online-Zugang:	Volltext
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