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KASCH Protocols and Guidelines for Lysosomal Diseases

Protocol for Lysosomal Diseases in Patients Started ​on Enzyme Replacement Therapy (ERT)

This page is for healthcare professionals dealing with children who have lysosomal diseases.

 
Mucopolysaccharidosis type I
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Mucopolysaccharidosis type II
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Mucopolysacchardosis type IV
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MPS VI
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Fabry Disease
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Gaucher Disease
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Immune Tolerance Induction for CRIM
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Pompe Disease
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Emergency Protocols for Patients with Inborn Errors of Metabolism (IEM) Long Term Management

 
Argininosuccinate Lyase
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Maple Syrup Urine
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MCAD
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Methylmalonic Acidemia
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Propionic Acidemia
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Urea Cycle
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Emergency Protocols for Patients with Inborn Errors of Metabolism (IEM) Acute Management

 
Acute Management Of Primary Hyperammonemia
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Argininosuccinate Lyase Deficiency
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Maple Syrup Urine Disease
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MCAD
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MMA
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Propionic Acidemia
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Urea Cycle Diseases
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