Mucopolysaccharidoses (MPS) are lysosomal storage disorders due to impaired glycosaminoglycan degradation. Cardiac involvement is present in most patients with MPS although its clinical impact is still undetermined. Cardiovascular abnormalities were evaluated in 39 patients with MPS aged 4-22 years. Valvular lesions and different forms of cardiac involvement were detected. The most common lesion was thickening of the mitral valve with regurgitation or stenosis, regardless of the MPS type. Mitral valve thickening was observed in 23 patients, aortic valve thickening in 11 patients and congestive heart failure in only 1 patient with MPS III. The most severe changes were registered for MPS types I and II. Complete cardiological investigation sh...
Severe cardiac involvement is a common feature of mucopolysaccharidoses (MPS), but occurs only rarel...
Mucopolysaccharidosis (MPS) syndrome is an inherited metabolic disorder. In more than half of the pa...
Mucopolysaccharidoses (MPS) represent a group of rare lysosomal storage disorders, with a heterogene...
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 cardiovascular manifestations of the mucopolysaccharidoses (MPS) have not been well characterize...
<p>The paper gives the data available in the literature on the current classification, genealogy, cl...
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...
Mucopolysaccharidosis (MPS) IVA is a rare lysosomal storage disorder with multiple skeletal and non-...
Background: Mucopolysaccharidoses (MPSs) are a group of lysosomal storage disorders caused by the de...
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...
Mucopolysaccharidosis type VII (MPS VII) is caused by β-glucuronidase deficiency, resulting in lysos...
textabstractWe determined the cardiologic features of children with MPS I, II and VI, and evaluated ...
Severe cardiac involvement is a common feature of mucopolysaccharidoses (MPS), but occurs only rarel...
Mucopolysaccharidosis (MPS) syndrome is an inherited metabolic disorder. In more than half of the pa...
Mucopolysaccharidoses (MPS) represent a group of rare lysosomal storage disorders, with a heterogene...
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 cardiovascular manifestations of the mucopolysaccharidoses (MPS) have not been well characterize...
<p>The paper gives the data available in the literature on the current classification, genealogy, cl...
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...
Mucopolysaccharidosis (MPS) IVA is a rare lysosomal storage disorder with multiple skeletal and non-...
Background: Mucopolysaccharidoses (MPSs) are a group of lysosomal storage disorders caused by the de...
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...
Mucopolysaccharidosis type VII (MPS VII) is caused by β-glucuronidase deficiency, resulting in lysos...
textabstractWe determined the cardiologic features of children with MPS I, II and VI, and evaluated ...
Severe cardiac involvement is a common feature of mucopolysaccharidoses (MPS), but occurs only rarel...
Mucopolysaccharidosis (MPS) syndrome is an inherited metabolic disorder. In more than half of the pa...
Mucopolysaccharidoses (MPS) represent a group of rare lysosomal storage disorders, with a heterogene...