bilateral striopallidodentate calcinosis | ClinicalTrials HQ

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Trial	Conditions	Status	Phase	Updated	More info	NCT ID
Treatment of Ectopic Calcification in Fahr's Disease or Syndrome	bilateral striopallidodentate calcinosis	Recruiting	Phase 2	2026-03-02		NCT05662111
Longitudinal Study of Ultra-rare Inherited Metabolic and Degenerative Neurological Diseases.	2-hydroxyglutaric aciduria, Alexander disease, Brain Diseases, Metabolic, Brain Diseases, Metabolic, Inborn, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Cysts, Digestive System Diseases, Disease Attributes, Hereditary Central Nervous System Demyelinating Diseases, Krabbe disease, Leukoencephalopathies, Lipid Metabolism Disorders, Lipid Metabolism, Inborn Errors, Lysosomal Storage Diseases, Nervous System, Neurobehavioral Manifestations, Neurologic Manifestations, Nutritional and Metabolic Diseases, Pathologic Processes, Pathological Conditions, Anatomical, Pathological Conditions, Signs and Symptoms, Pelizaeus-Merzbacher spectrum disorder, Peroxisomal Disorders, Rare Diseases, Sulfatidosis, Undiagnosed Diseases, Wilson disease, X-linked disease, adrenal gland disorder, adrenocortical insufficiency, adrenoleukodystrophy, basal ganglia disorder, bilateral striopallidodentate calcinosis, brain disorder, central nervous system disorder, cerebrotendinous xanthomatosis, demyelinating disease, endocrine system disorder, hereditary disease, inborn errors of metabolism, inborn metal metabolism disorder, inherited neurodegenerative disorder, intellectual disability, liver disorder, lysosomal lipid storage disorder, lysosomal storage disease, metabolic disease, metachromatic leukodystrophy, methylmalonic aciduria and homocystinuria, movement disorder, neoplasm, nervous system disorder, neurodegenerative disease, polycystic lipomembranous osteodysplasia with sclerosing leukoencephaly, sphingolipidosis, xanthomatosis	Recruiting	Not stated	2024-11-19		NCT04880356