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Snijders Blok-Campeau syndrome

MONDO:0032600

Also known as: CHD3-related developmental delay-speech delay-intellectual disability-abnormalities of vision-facial dysmorphism syndrome, intellectual developmental disorder with macrocephaly, speech delay, and dysmorphic facies, SNIBCPS, SNIJDERS BLOK-CAMPEAU SYNDROME

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

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Broader categories

Disease (679) Hereditary disease (176) Human disease (14) Disease of genetic or genomic mechanism (2) Disease by etiologic mechanism (0)
Terminated 1
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  • One-shot gene editor aims to correct a brain disorder at its source

    ⭐️ CURE ⭐️ Terminated

    This trial tests whether a single injection of a gene-editing tool can safely correct a specific mutation in the CHD3 gene that causes Snijders Blok-Campeau syndrome, a condition marked by developmental delay and intellectual disability. The gene editor is delivered directly into…

    Phase: EARLY_PHASE1 • Sponsor: Yongguo Yu • Aim: ⭐️ CURE ⭐️

    Last updated Aug 01, 2026 00:00 UTC

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