Hereditary spastic paraplegia 13
MONDO:0011532Any hereditary spastic paraplegia in which the cause of the disease is a mutation in the HSPD1 gene.
Also known as: HSPD1 hereditary spastic paraplegia, SPG13, hereditary spastic paraplegia caused by mutation in HSPD1, hereditary spastic paraplegia type 13, autosomal dominant spastic paraplegia type 13, spastic paraplegia 13, spastic paraplegia 13, autosomal dominant
2 clinical trials for this condition and its sub-types, 0 tagged with Hereditary spastic paraplegia 13 itself.
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Can ultrasound make botox injections more precise for stiff muscles?
Disease control Recruiting nowThis trial tests whether using ultrasound to guide botulinum toxin injections into spastic leg muscles works better than the standard method of relying on touch and anatomical landmarks. Researchers will give 40 adults with spastic paraplegia two rounds of injections, one with ea…
Phase 4 • Sponsor: Universidade Federal Fluminense • Aim: Disease control
Last updated Sep 05, 2026 00:00 UTC
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Can a massive natural history study unlock the secrets of rare movement disorders?
Knowledge-focused Recruiting nowThis study follows thousands of people with ataxia, hereditary spastic paraplegia, and spastic ataxia, rare conditions that cause progressive problems with walking, balance, and coordination. Researchers will track how symptoms evolve using clinical exams, patient reports, digita…
Sponsor: Heidelberg University • Aim: Knowledge-focused
Last updated Sep 03, 2026 00:00 UTC