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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 Click Here Mucopolysaccharidosis type II Click HereMucopolysacchardosis type IVClick HereMPS VIClick Here
Fabry Disease Click HereGaucher DiseaseClick HereImmune Tolerance Induction for CRIMClick HerePompe DiseaseClick Here

Emergency Protocols for Patients with Inborn Errors of Metabolism (IEM) Long Term Management


Argininosuccinate LyaseClick HereMaple-Syrup-UrineClick HereMCADClick HereMethylmalonic AcidemiaClick Here
Propionic AcidemiaClick HereUrea CycleClick Here

Emergency Protocols for Patients with Inborn Errors of Metabolism (IEM) Acute Management

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

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Last Modified

9/6/2022 2:11 PM

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