NGS-Based Genetic Approach to Identify Rare Lysosomal Storage Disorders in Patients With Neurological Manifestations
NGS-Based Genetic Approach to Identify Rare Lysosomal Storage Disorders in Patients With Neurological Manifestations
Active, not recruiting · NCT07863479 · Registry updated 2026-10-07Clinical trials
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| Trial | Conditions | Status | Phase | Updated | More info | NCT ID |
|---|---|---|---|---|---|---|
| NGS-Based Genetic Approach to Identify Rare Lysosomal Storage Disorders in Patients With Neurological Manifestations | Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Nutritional and Metabolic Diseases, hereditary disease, inborn errors of metabolism, lysosomal storage disease, metabolic disease | Active, not recruiting | Not applicable | 2026-10-07 | NCT07863479 |
2 results · Page 1 of 1
Organizations
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| Organizations | Linked trials |
|---|---|
| Fondazione IRCCS Ca' Granda, Ospedale Maggiore Policlinico | 90 |
| Sanofi | 254 |
1 results · Page 1 of 1
Research sites
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| Research sites | City | Country | Linked trials |
|---|---|---|---|
| S.C. Neurologia, Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico | Milan | Italy | 1 |