Autosomal recessive complex spastic paraplegia type 9B
MONDO:0014702Any autosomal recessive complex spastic paraplegia in which the cause of the disease is a mutation in the ALDH18A1 gene.
Also known as: ALDH18A1 autosomal recessive complex spastic paraplegia, AR-SPG9B, SPG9B, autosomal recessive complex spastic paraplegia caused by mutation in ALDH18A1, hereditary spastic paraplegia type 9B, hereditary spastic paraplegia 9B, spastic paraplegia 9B, autosomal recessive
2 clinical trials for this condition and its sub-types, 0 tagged with Autosomal recessive complex spastic paraplegia type 9B 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