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Sly syndrome
(redirected from Mucopolysaccharidosis type VII)

   Also found in: Dictionary/thesaurus, Acronyms, Encyclopedia, Wikipedia 0.01 sec.
Sly syndrome
[slī]
Etymology: William S. Sly, American physician, b. 1932
a mucopolysaccharidosis caused by deficiency of an enzyme important for the degradation of various mucopolysaccharides. It is characterized by excretion of mucopolysaccharides in the urine and by granular inclusions in granulocytes. Onset is between 1 and 2 years of age, with mild to moderate Hurler-like features, including dysostosis multiplex, pigeon breast, organomegaly, cardiac murmurs, short stature, and moderate mental retardation. Milder forms exist. Also called MPS VII.

sly syndrome
human mucopolysaccharidosis, analogous to β-glucuronidase deficiency mucopolysaccharidosis in experimental dogs.


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With the exception of the formation of liver tumors in some mice, the results of the gene therapy experiments in mice engineered to mimic a human disease called mucopolysaccharidosis type VII were encouraging.
The mice were born with mucopolysaccharidosis Type VII, a disfiguring and eventually fatal disease caused by mutations in the genes that code for beta-glucuronidase.
In humans the same disease, known as mucopolysaccharidosis type VII (MPS VII), remains largely incurable.
 
 
Mucopolysaccharidosis type I Hurler syndrome
Mucopolysaccharidosis type I Hurler syndrome
Mucopolysaccharidosis type I Hurler syndrome
Mucopolysaccharidosis type I Hurler/Scheie syndrome
Mucopolysaccharidosis type I Hurler/Scheie syndrome
Mucopolysaccharidosis type I Hurler/Scheie syndrome
Mucopolysaccharidosis type I Scheie syndrome
Mucopolysaccharidosis type I Scheie syndrome
Mucopolysaccharidosis type I Scheie syndrome
Mucopolysaccharidosis Type II
Mucopolysaccharidosis Type II
Mucopolysaccharidosis type II Hunter syndrome- mild form
Mucopolysaccharidosis type II Hunter syndrome- mild form
Mucopolysaccharidosis type II Hunter syndrome- mild form
Mucopolysaccharidosis type II Hunter syndrome- severe form
Mucopolysaccharidosis type II Hunter syndrome- severe form
Mucopolysaccharidosis type II Hunter syndrome- severe form
Mucopolysaccharidosis type IV-A Morquio syndrome
Mucopolysaccharidosis type IV-A Morquio syndrome
Mucopolysaccharidosis type IV-A Morquio syndrome
Mucopolysaccharidosis type IV-B
Mucopolysaccharidosis type IV-B
Mucopolysaccharidosis type IV-B
Mucopolysaccharidosis Type IX
Mucopolysaccharidosis type V
Mucopolysaccharidosis type V
Mucopolysaccharidosis type V
Mucopolysaccharidosis type VI Maroteaux-Lamy - severe, intermediate
Mucopolysaccharidosis type VI Maroteaux-Lamy - severe, intermediate
Mucopolysaccharidosis type VI Maroteaux-Lamy - severe, intermediate
Mucopolysaccharidosis type VII
Mucopolysaccharidosis type VII Sly syndrome
mucopolysaccharidosis V
Mucopolysaccharidosis VI
Mucopolysaccharidosis VI
Mucopolysaccharidosis VI
Mucopolysaccharidosis vii
Mucopolysaccharidosis, type I
Mucopolysaccharidosis, type II
Mucopolysaccharidosis, type II
Mucopolysaccharidosis-Mild Form
mucopolysacchariduria
Mucopolysaccharoidosis
Mucopolysaccharoidosis
Mucopolysaccharoidosis
mucoprotein
mucoprotein
mucoprotein
Mucoproteins
Mucoproteins
Mucoproteins
mucopurulent
mucopurulent
mucopurulent
Mucopurulent cervicitis
Mucopurulent cervicitis
Mucopurulent cervicitis
Mucopurulent cervicitis
mucopus
mucor
mucor
 
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