Autosomal dominant spastic paraplegia type 9
MONDO:0015091Any autosomal dominant complex spastic paraplegia in which the cause of the disease is a mutation in the ALDH18A1 gene.
Also known as: ALDH18A1 autosomal dominant complex spastic paraplegia, SPG9, autosomal dominant complex spastic paraplegia caused by mutation in ALDH18A1, cataracts-motor neuropathy-short stature-skeletal anomalies syndrome, spastic paraparesis-amyopathy-cataracts-gastroesophageal reflux syndrome, autosomal dominant spastic paraparesis, bilateral cataracts, gastroesophageal reflux, and spastic paraparesis with amyotrophy, cataracts, motor neuronopathy, short stature and skeletal abnormalities
2 clinical trials for this condition and its sub-types, 0 tagged with Autosomal dominant spastic paraplegia type 9 itself.
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Browse by category →Sub-types of Autosomal dominant spastic paraplegia type 9
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Hereditary spastic paraplegia 9A 0 trials
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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