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Hypomyelinating leukodystrophy 4

MONDO:0012824

Any leukodystrophy in which the cause of the disease is a mutation in the HSPD1 gene.

Also known as: HLD4, HSPD1 leukodystrophy, MitCHAP60 disease, Pelizaeus-Merzbacher-like disease due to HSPD1 mutation, hypomyelinating leukodystrophy type 4, leukodystrophy caused by mutation in HSPD1, leukodystrophy, hypomyelinating, type 4, mitochondrial HSP60 chaperonopathy

16 clinical trials for this condition and its sub-types.

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Broader categories

Disease (618) Nervous system disorder (217) Hereditary disease (172) Neurodegenerative disease (155) Central nervous system disorder (97) Human disease (14) Inherited neurodegenerative disorder (10) Hereditary neurological disease (5) Leukodystrophy (5) Disease of genetic or genomic mechanism (2)
Trials to join now! 7 Not yet recruiting 1 Not yet finished but already full! 2 Completed 6
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  • Could a zapping cap boost memory? small study tests brain stimulation for cognitive decline

    Symptom relief Not yet recruiting

    This pilot study will test whether a non-invasive brain stimulation technique called transcranial alternating current stimulation (tACS) can improve working memory in 30 adults with mild cognitive impairment or traumatic brain injury. Participants will receive low-level electrica…

    Phase: NA • Sponsor: Sunnybrook Health Sciences Centre • Aim: Symptom relief

    Last updated Jun 27, 2026 12:28 UTC

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