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Leukodystrophy, demyelinating, adult-onset, autosomal dominant, typical

MONDO:0700295

1 clinical trial for this condition and its sub-types.

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Broader categories

Disease (680) Nervous system disorder (231) Hereditary disease (176) Neurodegenerative disease (171) Central nervous system disorder (107) Human disease (14) Chromosomal disorder (12) Inherited neurodegenerative disorder (10) Hereditary neurological disease (6) Leukodystrophy (5)

Trials to join now! 1

Scientists hunt for 'Modifier Genes' that could explain why some LMNA patients fare better than others

Knowledge-focused Recruiting now

This study aims to identify genetic factors that affect how severe muscle and heart problems become in people with LMNA gene mutations. Researchers will collect skin and muscle samples from 40 participants and use advanced DNA and RNA analysis to look for protective or aggravatin…

Phase: NA • Sponsor: Institut National de la Santé Et de la Recherche Médicale, France • Aim: Knowledge-focused

Last updated Jun 27, 2026 09:10 UTC