Early diagnosis and management of cardiac manifestations in mucopolysaccharidoses: a practical guide for paediatric and adult cardiologists

Abstract Mucopolysaccharidoses (MPS) are a group of hereditary disorders caused by lysosomal storage of glycosaminoglycans (GAGs) and characterized by a wide variability of phenotypes from severe fetal-neonatal forms to attenuated diseases diagnosed in adult individuals. The clinical picture general...

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Ngā kaituhi matua: Lucia Boffi (Author), Pierluigi Russo (Author), Giuseppe Limongelli (Author)
Hōputu: Pukapuka
I whakaputaina: BMC, 2018-11-01T00:00:00Z.
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