Lysosomal storage disease with skeletal involvement

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Sub-types of Lysosomal storage disease with skeletal involvement

• Mucopolysaccharidosis type 2 25 trials
  2 sub-types

  • Mucopolysaccharidosis type 2, severe form 1 trial
  • Mucopolysaccharidosis type 2, attenuated form 0 trials
• Mucopolysaccharidosis type 4A 8 trials
• Mucopolysaccharidosis type 6 8 trials
  2 sub-types

  • Mucopolysaccharidosis type 6, rapidly progressing 0 trials
  • Mucopolysaccharidosis type 6, slowly progressing 0 trials
• Mucopolysaccharidosis type 7 8 trials
• Mucopolysaccharidosis type 3A 7 trials
• Hurler syndrome 6 trials
• Mucopolysaccharidosis type 3B 6 trials
• Alpha-mannosidosis 5 trials
  3 sub-types

  • Alpha-mannosidosis type 1 0 trials
  • Alpha-mannosidosis, adult form 0 trials
  • Alpha-mannosidosis, infantile form 0 trials
• Aspartylglucosaminuria 4 trials
• Mucosulfatidosis 4 trials
• GM1 gangliosidosis type 1 3 trials
• Hurler-Scheie syndrome 2 trials
• Fucosidosis 2 trials
• Galactosialidosis 2 trials
• Mucopolysaccharidosis type 3C 2 trials
• Scheie syndrome 1 trial
• GNPTG-mucolipidosis 0 trials
• Beta-mannosidosis 0 trials
• Free sialic acid storage disease, infantile form 0 trials
• Mucolipidosis type II 0 trials
• Mucolipidosis type III, alpha/beta 0 trials
• Mucopolysaccharidosis type 3D 0 trials
• Mucopolysaccharidosis type 4B 0 trials
• Mucopolysaccharidosis-plus syndrome 0 trials
• Sialidosis type 2 0 trials
  2 sub-types

  • Congenital sialidosis type 2 0 trials
  • Juvenile sialidosis type 2 0 trials