Overview
Lysosomal storage disease is a disorder.
Auto-generated from clinical reference data. Not a substitute for medical advice.
Treatments & Interventions
Research Evidence
Peer-reviewed studies linked via MeSH term "Lysosomal Storage Diseases" from the MEDLINE/PubMed database.
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Systematic Review of Genetic Substrate Reduction Therapy in Lysosomal Storage Diseases: Opportunities, Challenges and Delivery Systems.
[object Object], [object Object], [object Object] et al. · BioDrugs · 2024
A systematic review on the birth prevalence of metachromatic leukodystrophy.
[object Object], [object Object], [object Object] et al. · Orphanet J Rare Dis · 2024
Neuropsychology assessment and outcomes in adult mucopolysaccharidosis - A systematic review as the first step to service development in a large tertiary Lysosomal Storage Disorders centre.
[object Object], [object Object], [object Object] et al. · Mol Genet Metab · 2023
PMID: 36709537Meta-Analysis
Hypersensitivity reaction during enzyme replacement therapy in lysosomal storage disorders. A systematic review of desensitization strategies.
[object Object], [object Object], [object Object] et al. · Pediatr Allergy Immunol · 2023
PMID: 37366214Meta-Analysis
Patient-reported outcomes in Gaucher's disease: a systematic review.
[object Object], [object Object], [object Object] et al. · Orphanet J Rare Dis · 2023
The surgical management of spinal disorders in lysosomal storage diseases: a systematic review.
[object Object], [object Object] · ANZ J Surg · 2022
PMID: 34984775Meta-Analysis
Lysosomal storage disorders as an etiology of nonimmune hydrops fetalis: A systematic review.
[object Object], [object Object], [object Object] et al. · Clin Genet · 2021
Mechanisms of Neutralizing Anti-drug Antibody Formation and Clinical Relevance on Therapeutic Efficacy of Enzyme Replacement Therapies in Fabry Disease.
[object Object], [object Object] · Drugs · 2021
The burden of rare damaging variants in hereditary atypical parkinsonism genes is increased in patients with Parkinson's disease.
[object Object], [object Object], [object Object] et al. · Neurobiol Aging · 2021
PMID: 33423827Meta-Analysis
The natural history of Type 1 infantile GM1 gangliosidosis: A literature-based meta-analysis.
[object Object], [object Object], [object Object] et al. · Mol Genet Metab · 2020
Search all PubMed articles for Lysosomal storage disease
Research data from MEDLINE/PubMed
Related Conditions
Mucopolysaccharidosis(child)
Mucolipidosis(child)
Gangliosidosis(child)
Neuronal ceroid lipofuscinosis(child)
Cystinosis(child)
Sphingolipidosis(child)
Disorder of sialic acid metabolism(child)
Danon disease(child)
LAL (Lysosomal acid lipase) deficiency(child)
Oligosaccharidosis(child)
Storage disease(parent)
Enzymopathy(parent)
Quick Facts
- SNOMED CT
- 28821000119102
- UMLS CUI
- C0085078
- Fully Specified Name
- Lysosomal storage disease (disorder)
- Specialists
- 0
- Diagnostic Biomarkers
- 0
- Known Treatments
- 1
Medical Disclaimer
This information is for educational purposes only and does not constitute medical advice, diagnosis, or treatment. Always consult with a qualified healthcare provider regarding any medical condition or treatment plan.
Clinical content is derived from the SNOMED CT clinical ontology and curated medical knowledge graphs.