Natural History Study of Patients with HPDL Mutations | ClinicalTrials HQ

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Trial	Conditions	Status	Phase	Updated	More info	NCT ID
Natural History Study of Patients with HPDL Mutations	Brain Diseases, Metabolic, Congenital Abnormalities, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Leukoencephalopathies, Neurologic Manifestations, Nutritional and Metabolic Diseases, Paraplegia, Spastic, Pathological Conditions, Signs and Symptoms, Signs and Symptoms, brain disorder, central nervous system disorder, central nervous system malformation, hereditary disease, hereditary motor and sensory neuropathy, hereditary spastic paraplegia, inborn mitochondrial metabolism disorder, inborn mitochondrial myopathy, inherited neurodegenerative disorder, metabolic disease, mitochondrial encephalomyopathy, muscle tissue disorder, musculoskeletal system disorder, nervous system disorder, neurodegenerative disease, neuromuscular disease, palsy, paraplegia, peripheral nervous system disorder, polyneuropathy	Recruiting	Not stated	2025-03-30		NCT05848271

4 results · Page 1 of 1

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Organizations	Linked trials
Heinrich-Heine University, Duesseldorf	71
New York University	90
University of California, San Diego	337
Universität Tübingen	12

1 results · Page 1 of 1

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Research sites	City	Country	Linked trials
Eun Hae Lee	San Diego	United States	1