The cardiovascular manifestations of the mucopolysaccharidoses (MPS) have not been well characterized. We studied nine children with various forms of MPS, using noninvasive cardiac diagnostic techniques. The echocardiograms of two brothers with Type I H/S MPS showed slow mitral valve early diastolic closure velocities (MVEDC) (18, 29 mm/sec) consistent with mitral stenosis. Each had a soft opening snap, low frequency presystolic murmurs and X-ray evidence of calcific mitral stenosis. Three patients with Type II A MPS had echocardiographic evidence of impaired left ventricular function, suggesting the presence of myocardial damage. One of these had an abnormal electrocardiogram; none had murmurs. No cardiac ab-normalities were discovered in ...
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...
Mucopolysaccharidoses (MPS) represent a group of rare lysosomal storage disorders, with a heterogene...
Mucopolysaccharidoses (MPS) are lysosomal storage disorders due to impaired glycosaminoglycan degrad...
The mucopolysaccharidoses (MPSs) are inherited lysosomal storage disorders caused by the absence of ...
Background. Cardiac involvement in patients with mucopolysaccharidosis (MPS) type I, or Hurler syndr...
Mucopolysaccharidoses (MPS) are inherited lysosomal storage disorders caused by deficiency of requir...
Principle Mucopolysaccharidosis is an inborn error of metabolism causing glucosaminoglycans tissue s...
Mucopolysaccharidoses (MPS) are a group of hereditary disorders caused by lysosomal storage of glyco...
Mucopolysaccharidosis (MPS) IVA is a rare lysosomal storage disorder with multiple skeletal and non-...
textabstractWe determined the cardiologic features of children with MPS I, II and VI, and evaluated ...
Mucopolysaccharidosis (MPS) syndrome is an inherited metabolic disorder. In more than half of the pa...
Mucopolysaccharidoses, a rare inherited disorder of lysosomal storage, account for less than 0.1% of...
Through this case, we want to highlight, that in patients with mucopolysaccharoidosis (MPS), coronar...
Severe cardiac involvement is a common feature of mucopolysaccharidoses (MPS), but occurs only rarel...
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...
Mucopolysaccharidoses (MPS) represent a group of rare lysosomal storage disorders, with a heterogene...
Mucopolysaccharidoses (MPS) are lysosomal storage disorders due to impaired glycosaminoglycan degrad...
The mucopolysaccharidoses (MPSs) are inherited lysosomal storage disorders caused by the absence of ...
Background. Cardiac involvement in patients with mucopolysaccharidosis (MPS) type I, or Hurler syndr...
Mucopolysaccharidoses (MPS) are inherited lysosomal storage disorders caused by deficiency of requir...
Principle Mucopolysaccharidosis is an inborn error of metabolism causing glucosaminoglycans tissue s...
Mucopolysaccharidoses (MPS) are a group of hereditary disorders caused by lysosomal storage of glyco...
Mucopolysaccharidosis (MPS) IVA is a rare lysosomal storage disorder with multiple skeletal and non-...
textabstractWe determined the cardiologic features of children with MPS I, II and VI, and evaluated ...
Mucopolysaccharidosis (MPS) syndrome is an inherited metabolic disorder. In more than half of the pa...
Mucopolysaccharidoses, a rare inherited disorder of lysosomal storage, account for less than 0.1% of...
Through this case, we want to highlight, that in patients with mucopolysaccharoidosis (MPS), coronar...
Severe cardiac involvement is a common feature of mucopolysaccharidoses (MPS), but occurs only rarel...
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...
Mucopolysaccharidoses (MPS) represent a group of rare lysosomal storage disorders, with a heterogene...