La maladie de Sanfilippo ou mucopolysaccharidose de type III (MPS III) est une maladie génétique rare. Il s agit d une maladie lysosomale. Une anomalie dans le phénomène de dégradation de l héparane sulfate est à l origine de cette maladie. Cette anomalie aboutit à une accumulation de l héparane sulfate dans différents organes. Les patients présentent une agressivité, un sommeil perturbé, une hyperactivité ainsi qu une incoordination motrice. A l heure actuelle, il n existe pas de traitement spécifique de la maladie de Sanfilippo. La prise en charge consiste en un traitement symptomatique des différents troubles observés. Différentes stratégie thérapeutique sont étudiées mais seule la thérapie génique semble prometteuse.Sanfilippo syndrome ...
Mucopolysaccharidosis type IIIB (MPS IIIB, Sanfilippo syndrome type B) is a lysosomal storage disord...
Mucopolysaccharidosis type IIIB (MPS IIIB, Sanfilippo syndrome type B) is a lysosomal storage disord...
Mucopolysaccharidosis type IIIB (MPS IIIB, Sanfilippo syndrome type B) is a lysosomal storage disord...
Mucopolysaccharidosis type III (MPS III, Sanfilippo syndrome) is an autosomal recessive disorder, ca...
Mucopolysaccharidoses (MPS) are severe, inherited metabolic disorders caused by defective lysosomal ...
Anthony O FedeleLysosomal Diseases Research Unit, South Australian Health and Medical Research Insti...
Introduction: Mucopolysaccharidosis type III (MPS III, Sanfilippo syndrome) is a rare autosomal rece...
Mucopolysaccharidosis type III, also known as MPS III or Sanfilippo syndrome, is a lysosomal storage...
Mucopolysaccharidosis III D (Sanfilippo disease type D, MPS IIID) is a rare autosomal recessive lyso...
Contains fulltext : 89263.pdf (publisher's version ) (Closed access)Mucopolysaccha...
Mucopolysaccharidosis III D (Sanfilippo disease type D, MPS IIID) is a rare autosomal recessive lyso...
Abstract Background Sanfilippo syndrome (mucopolysaccharidosis type III; MPS III) is an inherited mo...
Mucopolysaccharidosis type III (MPS III), or Sanfilippo syndrome, is a lysosomal storage disease in ...
Mucopolysaccharidosis type IIIB (MPS IIIB, Sanfilippo syndrome type B) is a lysosomal storage disord...
Mucopolysaccharidosis type IIIB (MPS IIIB, Sanfilippo syndrome type B) is a lysosomal storage disord...
Mucopolysaccharidosis type IIIB (MPS IIIB, Sanfilippo syndrome type B) is a lysosomal storage disord...
Mucopolysaccharidosis type IIIB (MPS IIIB, Sanfilippo syndrome type B) is a lysosomal storage disord...
Mucopolysaccharidosis type IIIB (MPS IIIB, Sanfilippo syndrome type B) is a lysosomal storage disord...
Mucopolysaccharidosis type III (MPS III, Sanfilippo syndrome) is an autosomal recessive disorder, ca...
Mucopolysaccharidoses (MPS) are severe, inherited metabolic disorders caused by defective lysosomal ...
Anthony O FedeleLysosomal Diseases Research Unit, South Australian Health and Medical Research Insti...
Introduction: Mucopolysaccharidosis type III (MPS III, Sanfilippo syndrome) is a rare autosomal rece...
Mucopolysaccharidosis type III, also known as MPS III or Sanfilippo syndrome, is a lysosomal storage...
Mucopolysaccharidosis III D (Sanfilippo disease type D, MPS IIID) is a rare autosomal recessive lyso...
Contains fulltext : 89263.pdf (publisher's version ) (Closed access)Mucopolysaccha...
Mucopolysaccharidosis III D (Sanfilippo disease type D, MPS IIID) is a rare autosomal recessive lyso...
Abstract Background Sanfilippo syndrome (mucopolysaccharidosis type III; MPS III) is an inherited mo...
Mucopolysaccharidosis type III (MPS III), or Sanfilippo syndrome, is a lysosomal storage disease in ...
Mucopolysaccharidosis type IIIB (MPS IIIB, Sanfilippo syndrome type B) is a lysosomal storage disord...
Mucopolysaccharidosis type IIIB (MPS IIIB, Sanfilippo syndrome type B) is a lysosomal storage disord...
Mucopolysaccharidosis type IIIB (MPS IIIB, Sanfilippo syndrome type B) is a lysosomal storage disord...
Mucopolysaccharidosis type IIIB (MPS IIIB, Sanfilippo syndrome type B) is a lysosomal storage disord...
Mucopolysaccharidosis type IIIB (MPS IIIB, Sanfilippo syndrome type B) is a lysosomal storage disord...