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Hereditary spastic paraplegia 11
MONDO:0011445Any hereditary spastic paraplegia in which the cause of the disease is a mutation in the SPG11 gene.
Also known as: HSP-TCC, Nakamura-Osame syndrome, SPG11, SPG11 hereditary spastic paraplegia, autosomal recessive spastic paraplegia type 11, hereditary spastic paraplegia caused by mutation in SPG11, hereditary spastic paraplegia type 11, spastic paraplegia-intellectual disability-thin corpus callosum syndrome
15 clinical trials for this condition and its sub-types.
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AI boosts brain scan accuracy in massive new trial
Diagnosis ENROLLING_BY_INVITATIONThis study tests whether an AI tool can help radiologists read brain CT and MRI scans more accurately and quickly. Researchers will compare how well doctors, AI alone, and doctors using AI together can spot abnormalities, urgent findings, and classify diseases. The goal is to red…
Sponsor: Yaou Liu • Aim: Diagnosis
Last updated Jun 27, 2026 11:00 UTC
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Could a headset at home boost brain recovery? new study tests tDCS for stroke, tumors, and neurodegeneration
Symptom relief ENROLLING_BY_INVITATIONThis study tests whether a home-based brain stimulation device (tDCS) combined with activity therapy can help improve cognitive and language problems in people with stroke, brain tumors, or neurodegenerative conditions like Parkinson's or Alzheimer's. Fifty-five participants will…
Phase: NA • Sponsor: Mayo Clinic • Aim: Symptom relief
Last updated Jun 27, 2026 09:00 UTC