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A disorder that involves more than one phenotype associated with the central nervous system, including but not limited to intellectual disability, autism, and seizures (epilepsy), and also a distinctive pattern of other features including dysmorphisms and/or congenital malformations.
No clinical trials have been registered for syndromic complex neurodevelopmental disorder.
4 publications have been identified in PubMed for syndromic complex neurodevelopmental disorder. Research spans Review / Meta-Analysis (50%), Case Report / Case Series (25%), and Basic Science / Preclinical (25%).
Thodeson D (2026). [PMID: 41751547](https://pubmed.ncbi.nlm.nih.gov/41751547/). *Genes*. [Review / Meta-Analysis]
Briot K (2026). [PMID: 41746411](https://pubmed.ncbi.nlm.nih.gov/41746411/). *Journal of neural transmission (Vienna, Austria : 1996)*. [Case Report / Case Series]
Rezazadeh S (2025). [PMID: 40469903](https://pubmed.ncbi.nlm.nih.gov/40469903/). *Frontiers in molecular neuroscience*. [Basic Science / Preclinical]
Cordova I (2024). [PMID: 38674358](https://pubmed.ncbi.nlm.nih.gov/38674358/). *Genes*. [Review / Meta-Analysis]
Data assembled from 2 of 12 sources · Last updated Sep 19, 2026, 1:53 PM UTC