Principle Mucopolysaccharidosis is an inborn error of metabolism causing glucosaminoglycans tissue storage. Cardiovascular involvement is variable but contributes significantly towards the morbidity and mortality of the patients. Objective To characterise the echocardiographic abnormalities in children and adolescents with different types of mucopolysaccharidosis. Method Echocardiograms and medical records of 28 patients aged 2–14 years, seen from 2003 to 2005, were revised. At that time, the enzymatic replacement therapy was still not available in our institution.Results Echocardiographic alterations were detected in 26 patients (93 per cent), whereas 16 (57 per cent) had abnormal auscultation, and only 6 (21 per cent) presented with cardi...
Background. Cardiac involvement in patients with mucopolysaccharidosis (MPS) type I, or Hurler syndr...
AbstractThrough this case, we want to highlight, that in patients with mucopolysaccharoidosis (MPS),...
<p>The paper gives the data available in the literature on the current classification, genealogy, cl...
Principle Mucopolysaccharidosis is an inborn error of metabolism causing glucosaminoglycans tissue s...
Mucopolysaccharidoses, a rare inherited disorder of lysosomal storage, account for less than 0.1% of...
Mucopolysaccharidoses (MPS) are lysosomal storage disorders due to impaired glycosaminoglycan degrad...
Mucopolysaccharidoses (MPS) are inherited lysosomal storage disorders caused by deficiency of requir...
The cardiovascular manifestations of the mucopolysaccharidoses (MPS) have not been well characterize...
textabstractWe determined the cardiologic features of children with MPS I, II and VI, and evaluated ...
Mucopolysaccharidoses, a rare inherited disorder of lysosomal storage, account for less than 0.1% of...
The mucopolysaccharidoses (MPSs) are inherited lysosomal storage disorders caused by the absence of ...
Mucopolysaccharidosis (MPS) IVA is a rare lysosomal storage disorder with multiple skeletal and non-...
The mucopolysaccharidoses (MPSs) are inherited lysosomal storage disorders caused by the absence of ...
Mucopolysaccharidoses (MPS) are a group of hereditary disorders caused by lysosomal storage of glyco...
The Mucopolysaccharidoses (MPS) are rare inherited metabolic disorders. They are characterized by th...
Background. Cardiac involvement in patients with mucopolysaccharidosis (MPS) type I, or Hurler syndr...
AbstractThrough this case, we want to highlight, that in patients with mucopolysaccharoidosis (MPS),...
<p>The paper gives the data available in the literature on the current classification, genealogy, cl...
Principle Mucopolysaccharidosis is an inborn error of metabolism causing glucosaminoglycans tissue s...
Mucopolysaccharidoses, a rare inherited disorder of lysosomal storage, account for less than 0.1% of...
Mucopolysaccharidoses (MPS) are lysosomal storage disorders due to impaired glycosaminoglycan degrad...
Mucopolysaccharidoses (MPS) are inherited lysosomal storage disorders caused by deficiency of requir...
The cardiovascular manifestations of the mucopolysaccharidoses (MPS) have not been well characterize...
textabstractWe determined the cardiologic features of children with MPS I, II and VI, and evaluated ...
Mucopolysaccharidoses, a rare inherited disorder of lysosomal storage, account for less than 0.1% of...
The mucopolysaccharidoses (MPSs) are inherited lysosomal storage disorders caused by the absence of ...
Mucopolysaccharidosis (MPS) IVA is a rare lysosomal storage disorder with multiple skeletal and non-...
The mucopolysaccharidoses (MPSs) are inherited lysosomal storage disorders caused by the absence of ...
Mucopolysaccharidoses (MPS) are a group of hereditary disorders caused by lysosomal storage of glyco...
The Mucopolysaccharidoses (MPS) are rare inherited metabolic disorders. They are characterized by th...
Background. Cardiac involvement in patients with mucopolysaccharidosis (MPS) type I, or Hurler syndr...
AbstractThrough this case, we want to highlight, that in patients with mucopolysaccharoidosis (MPS),...
<p>The paper gives the data available in the literature on the current classification, genealogy, cl...