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Significados de mucopolysaccharidosis em inglês

russo
мукополисахаридоз
português
mucopolissacaridose
espanhol
mucopolisacaridosis
catalão
mucopolisacaridosi

Lysosomal storage disease that involves the accumulation of glycosaminoglycans in the tissues and their excretion in the urine.

Termos relacionados
mucopolissacaridose
Sinônimos
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1
Read: MPs have a responsibility to the people, not their political parties.
The South African
2
Everyone knows that MPs from the governing parties will support government legislation.
Radio NZ
3
MPs later vote to extend the detention time limit to 28 days.
The Guardian
4
However, many MPs from across the political spectrum shared the Speaker's view.
The Guardian
5
Corbyn is under increasing pressure from MPs to support a second referendum.
The Guardian
1
Cardiac involvement has been reported in various mucopolysaccharidoses syndromes.
Pubmed
2
The mucopolysaccharidoses are a group of lysosomal storage disorders caused by defects in the degradation of glycosaminoglycans.
Pubmed
3
Pain is a common feature in mucopolysaccharidoses.
Pubmed
4
This case highlights the importance of early routine cardiac screening for conduction abnormalities and close follow-up in patients with mucopolysaccharidoses syndromes.
Pubmed
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.
Pubmed
Uso de mucopolysaccharidosis em inglês
1
These recommendations will help to obtain a complete and correct diagnosis of mucopolysaccharidosis, rendering also possible genetic counseling.
Pubmed
2
Background: Recent reports have shown a correlation between extensive Mongolian spots and mucopolysaccharidosis type II (Hunter syndrome).
Pubmed
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.
Pubmed
4
Hunter syndrome (mucopolysaccharidosis type II) is a rare and life-limiting multisystemic disorder with an X-linked recessive pattern of inheritance.
Pubmed
5
Renal failure was diagnosed in an 11-mo-old male domestic shorthair cat from a colony with mucopolysaccharidosis type I lysosomal storage disease.
Pubmed
6
We propose that serum levels of heparin cofactor II-thrombin complex may provide an important assessment and monitoring tool for patients with mucopolysaccharidosis.
Pubmed
7
The late-onset and variable severity of the symptoms may have precluded the description of such symptoms in parents of mucopolysaccharidosis IIIB cases.
Pubmed
8
The drug was also being tested in patients with Mucopolysaccharidosis Type I, an ultra-rare disorder.
Reuters
9
Haematopoietic stem cell transplantation is the treatment of choice for the severe form of Mucopolysaccharidosis Type I, or Hurler syndrome.
Pubmed
10
Mucopolysaccharidosis II is a lysosomal storage disorder caused by mutations in the IDS gene, including exonic alterations associated with aberrant splicing.
Pubmed
11
These recommendations will help to obtain a complete and correct diagnosis of mucopolysaccharidosis, rendering also possible genetic counseling.
Pubmed
12
Background: Recent reports have shown a correlation between extensive Mongolian spots and mucopolysaccharidosis type II (Hunter syndrome).
Pubmed
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.
Pubmed
14
Hunter syndrome (mucopolysaccharidosis type II) is a rare and life-limiting multisystemic disorder with an X-linked recessive pattern of inheritance.
Pubmed
15
Renal failure was diagnosed in an 11-mo-old male domestic shorthair cat from a colony with mucopolysaccharidosis type I lysosomal storage disease.
Pubmed
16
We propose that serum levels of heparin cofactor II-thrombin complex may provide an important assessment and monitoring tool for patients with mucopolysaccharidosis.
Pubmed
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Translations for mucopolysaccharidosis
Mucopolysaccharidosis ao longo do tempo