Hereditary spastic paraplegia 49
MONDO:0014016Any hereditary spastic paraplegia in which the cause of the disease is a mutation in the TECPR2 gene.
Also known as: SPG49, TECPR2 hereditary spastic paraplegia, autosomal recessive spastic paraplegia type 49, hereditary spastic paraplegia 49, hereditary spastic paraplegia caused by mutation in TECPR2, hereditary spastic paraplegia type 49, neuropathy, hereditary sensory and autonomic, type IX, with developmental delay, spastic paraplegia 49, autosomal recessive
2 clinical trials for this condition and its sub-types, 0 tagged with Hereditary spastic paraplegia 49 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