hereditary spastic paraplegia 26

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Trial	Conditions	Status	Phase	Updated	More info	NCT ID
Hereditary Spastic Paraplegia Genomic Sequencing Initiative (HSPseq)	Congenital Abnormalities, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Muscle Hypertonia, Muscle Spasticity, Neurologic Manifestations, Neuromuscular Manifestations, Pathological Conditions, Signs and Symptoms, Signs and Symptoms, central nervous system disorder, central nervous system malformation, hereditary disease, hereditary motor and sensory neuropathy, hereditary spastic paraplegia, hereditary spastic paraplegia 26, hereditary spastic paraplegia 3A, inherited neurodegenerative disorder, motor neuron disorder, movement disorder, muscle tissue disorder, musculoskeletal system disorder, nervous system disorder, neurodegenerative disease, neurodevelopmental disorder, neuromuscular disease, peripheral nervous system disorder, polyneuropathy, psychiatric disorder	Recruiting	Not stated	2026-03-18		NCT05354622

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