Please sign in to follow a disease.
Hereditary spastic paraplegia 52
MONDO:0013552Any hereditary spastic paraplegia in which the cause of the disease is a mutation in the AP4S1 gene.
Also known as: AP4S1 hereditary spastic paraplegia, SPG52, Spastic Paraplegia 52, hereditary spastic paraplegia 52, hereditary spastic paraplegia caused by mutation in AP4S1, hereditary spastic paraplegia type 52, cerebral palsy, spastic quadriplegic, 6, cerebral palsy, spastic quadriplegic, 6, formerly
15 clinical trials for this condition and its sub-types.
Follow this condition — get notified about new trialsBroader categories
-
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
-
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