Please sign in to follow a disease.
Autosomal recessive spastic paraplegia type 78
MONDO:0014975Any hereditary spastic paraplegia in which the cause of the disease is a mutation in the ATP13A2 gene.
Also known as: ATP13A2 hereditary spastic paraplegia, SPG78, hereditary spastic paraplegia caused by mutation in ATP13A2, spastic paraplegia 78, autosomal recessive, spastic paraplegia 78, autosomal recessive; SPG78
2 clinical trials for this condition and its sub-types, 0 tagged with Autosomal recessive spastic paraplegia type 78 itself.
Follow this condition to get notified about new trialsWhere it sits in the disease tree
Browse by category →-
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
-
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