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mucopolysaccharidosis IS

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mucopolysaccharidosis IS
Scheie's disease An AR mucopolysaccharidosis which, like Hurler syndrome, is characterized by a defect of α-l-iduronidase and excretion of ↑ dermatan sulfate in urine Clinical MPS-IS is the mildest form mucopolysaccharidosis; onset at age 4–5, including inguinal hernia, broad mouth with full lips, early onset corneal clouding, early onset of stiff joints, claw hands and deformed feet, aortic valve defects


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Mucopolysaccharide disease
Mucopolysaccharides
Mucopolysaccharides
Mucopolysaccharides
Mucopolysaccharides
Mucopolysaccharidoses
Mucopolysaccharidoses
Mucopolysaccharidoses
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Mucopolysaccharidosis i
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Mucopolysaccharidosis ii
Mucopolysaccharidosis ii
Mucopolysaccharidosis ii
Mucopolysaccharidosis iii
Mucopolysaccharidosis iii
mucopolysaccharidosis IS
Mucopolysaccharidosis iv
Mucopolysaccharidosis iv
Mucopolysaccharidosis type 3
Mucopolysaccharidosis type 3
Mucopolysaccharidosis type 3
Mucopolysaccharidosis type 4
Mucopolysaccharidosis type 4
Mucopolysaccharidosis type 4
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 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
 
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