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Significats de mucopolysaccharidosis en anglès
Lysosomal storage disease that involves the accumulation of glycosaminoglycans in the tissues and their excretion in the urine.
Termes relacionats
Sinònims
Examples for "mps"
Examples for "mps"
1
Read: MPs have a responsibility to the people, not their political parties.
2
Everyone knows that MPs from the governing parties will support government legislation.
3
MPs later vote to extend the detention time limit to 28 days.
4
However, many MPs from across the political spectrum shared the Speaker's view.
5
Corbyn is under increasing pressure from MPs to support a second referendum.
1
Cardiac involvement has been reported in various mucopolysaccharidoses syndromes.
2
The mucopolysaccharidoses are a group of lysosomal storage disorders caused by defects in the degradation of glycosaminoglycans.
3
Pain is a common feature in mucopolysaccharidoses.
4
This case highlights the importance of early routine cardiac screening for conduction abnormalities and close follow-up in patients with mucopolysaccharidoses syndromes.
5
Almost all known human sphingolipidoses, two mucopolysaccharidoses and aspartylglycosaminuria have so far been duplicated in mice and more are expected in the near future.
Ús de mucopolysaccharidosis en anglès
1
These recommendations will help to obtain a complete and correct diagnosis of mucopolysaccharidosis, rendering also possible genetic counseling.
2
Background: Recent reports have shown a correlation between extensive Mongolian spots and mucopolysaccharidosis type II (Hunter syndrome).
3
Cumulatively, our results allow transition to pre-clinical studies of SB-mediated alpha-L-iduronidase expression and correction of mucopolysaccharidosis type I in animal models.
4
Hunter syndrome (mucopolysaccharidosis type II) is a rare and life-limiting multisystemic disorder with an X-linked recessive pattern of inheritance.
5
Renal failure was diagnosed in an 11-mo-old male domestic shorthair cat from a colony with mucopolysaccharidosis type I lysosomal storage disease.
6
We propose that serum levels of heparin cofactor II-thrombin complex may provide an important assessment and monitoring tool for patients with mucopolysaccharidosis.
7
The late-onset and variable severity of the symptoms may have precluded the description of such symptoms in parents of mucopolysaccharidosis IIIB cases.
8
The drug was also being tested in patients with Mucopolysaccharidosis Type I, an ultra-rare disorder.
9
Haematopoietic stem cell transplantation is the treatment of choice for the severe form of Mucopolysaccharidosis Type I, or Hurler syndrome.
10
Mucopolysaccharidosis II is a lysosomal storage disorder caused by mutations in the IDS gene, including exonic alterations associated with aberrant splicing.
11
These recommendations will help to obtain a complete and correct diagnosis of mucopolysaccharidosis, rendering also possible genetic counseling.
12
Background: Recent reports have shown a correlation between extensive Mongolian spots and mucopolysaccharidosis type II (Hunter syndrome).
13
Cumulatively, our results allow transition to pre-clinical studies of SB-mediated alpha-L-iduronidase expression and correction of mucopolysaccharidosis type I in animal models.
14
Hunter syndrome (mucopolysaccharidosis type II) is a rare and life-limiting multisystemic disorder with an X-linked recessive pattern of inheritance.
15
Renal failure was diagnosed in an 11-mo-old male domestic shorthair cat from a colony with mucopolysaccharidosis type I lysosomal storage disease.
16
We propose that serum levels of heparin cofactor II-thrombin complex may provide an important assessment and monitoring tool for patients with mucopolysaccharidosis.
Sobre aquest terme
Translations for mucopolysaccharidosis
portuguès
espanyol
català
Mucopolysaccharidosis a través del temps