Hereditary spastic paraplegia 3A
MONDO:0008437Any hereditary spastic paraplegia in which the cause of the disease is a mutation in the ATL1 gene.
Also known as: ATL1 hereditary spastic paraplegia, FSP1, SPG3A, Strümpell disease, autosomal dominant spastic paraplegia type 3, hereditary spastic paraplegia caused by mutation in ATL1, hereditary spastic paraplegia type 3A, spastic Paraplegia 3A
2 clinical trials for this condition and its sub-types.
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Scientists hunt for genetic clues to rare paralysis disorder
Knowledge-focused Recruiting nowThis study aims to uncover the genetic causes of hereditary spastic paraplegia (HSP), a group of rare neurological diseases that cause progressive muscle stiffness and weakness. Researchers at Boston Children's Hospital will analyze DNA from 200 people with HSP to find genetic va…
Sponsor: Boston Children's Hospital • Aim: Knowledge-focused
Last updated Jun 27, 2026 11:03 UTC
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Scientists launch major effort to track rare nerve disease in children
Knowledge-focused Recruiting nowThis study collects health information and biological samples from up to 700 people under 30 with early-onset hereditary spastic paraplegia (HSP). Researchers aim to better understand how the disease progresses over time and create a registry for future studies. Participants prov…
Sponsor: Boston Children's Hospital • Aim: Knowledge-focused
Last updated Jun 27, 2026 11:02 UTC