Inclusion body myopathy with early-onset Paget disease with or without frontotemporal dementia 3
MONDO:0014179Any inclusion body myopathy with Paget disease of bone and frontotemporal dementia in which the cause of the disease is a mutation in the HNRNPA1 gene.
Also known as: HNRNPA1 inclusion body myopathy with Paget disease of bone and frontotemporal dementia, inclusion body myopathy with Paget disease of bone and frontotemporal dementia caused by mutation in HNRNPA1, inclusion body myopathy with early-onset Paget disease with or without frontotemporal dementia 3, inclusion body myopathy with early-onset Paget disease with or without frontotemporal dementia type 3, inclusion body myopathy with early-onset paget disease without frontotemporal dementia 3, IBMPFD3, multisystem Proteinopathy 3
11 clinical trials for this condition and its sub-types.
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Scientists map Brain's 'Roads' to predict dementia spread
Knowledge-focused ENROLLING_BY_INVITATIONThis study uses advanced MRI scans and genetic tests to track how neurodegenerative diseases like frontotemporal dementia and ALS spread across the brain's network. Researchers will follow 645 participants, including patients, family members, and healthy controls, for up to 2 yea…
Phase: NA • Sponsor: IRCCS San Raffaele • Aim: Knowledge-focused
Last updated Jun 27, 2026 12:29 UTC
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New study probes brain inflammation to unlock dementia mysteries
Knowledge-focused OngoingThis observational study looks at how brain inflammation contributes to frontotemporal lobar degeneration (FTLD), a group of disorders that cause dementia. Researchers will use advanced brain scans, blood tests, and spinal fluid analysis in 110 participants to find biomarkers tha…
Sponsor: Leiden University Medical Center • Aim: Knowledge-focused
Last updated Jun 26, 2026 15:38 UTC