brain small vessel disease 1 with or without ocular anomalies

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Trial	Conditions	Status	Phase	Updated	More info	NCT ID
COL4A1COL4A2: Study of Pathological Conditions Involving Multiple Organs Caused by Mutations in the COL4A1 and COL4A2 Genes	brain small vessel disease 1 with or without ocular anomalies	Recruiting	Not applicable	2026-01-30		NCT07374913
Taiwan Associated Genetic and Nongenetic Small Vessel Disease	Brain Diseases, Metabolic, Brain Diseases, Metabolic, Inborn, Cerebral Small Vessel Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Fabry disease, HTRA1-related autosomal dominant cerebral small vessel disease, Infarction, Lipid Metabolism Disorders, Lipid Metabolism, Inborn Errors, Lysosomal Storage Diseases, Nervous System, Necrosis, Nutritional and Metabolic Diseases, Pathologic Processes, Pathological Conditions, Signs and Symptoms, X-linked disease, brain disorder, brain infarction, brain ischemia, brain small vessel disease 1 with or without ocular anomalies, cardiovascular disorder, central nervous system disorder, cerebral arterial disease, cerebral infarction, cerebrovascular disorder, dementia, hereditary disease, inborn errors of metabolism, intracranial arterial disease, ischemic disease, lysosomal lipid storage disorder, lysosomal storage disease, metabolic disease, nervous system disorder, sphingolipidosis, stroke disorder, vascular dementia, vascular disorder	Recruiting	Not stated	2026-01-20		NCT05473637

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