Kisho is an information platform, not a medical provider. Nothing on this site constitutes medical advice, diagnosis, or treatment recommendations. All content is aggregated from publicly available sources (including ClinicalTrials.gov, PubMed, FDA.gov, and Orphanet) and is provided for informational purposes only. Clinical trial eligibility, treatment decisions, and any health-related actions should always be discussed with a qualified healthcare professional. Kisho does not endorse any specific therapy, organization, or clinical trial. Terms of use · Privacy policy
An autosomal dominant complex neurodevelopmental disorder in which the cause of the disease is a mutation in the MYH10 gene.
Biomarker and diagnostic research for MYH10-related neurodevelopmental disorder with congenital anomalies has been reported in the published literature.
No clinical trials have been registered for MYH10-related neurodevelopmental disorder with congenital anomalies.
202 publications have been identified in PubMed for MYH10-related neurodevelopmental disorder with congenital anomalies. Kisho has analyzed 82 by research type. Research spans Basic Science / Preclinical (32%), Case Report / Case Series (26%), and Review / Meta-Analysis (20%).
Research Type | Count | % of Total |
|---|---|---|
Laboratory research | 26 |
Data assembled from 2 of 12 sources · Last updated Sep 20, 2026, 8:31 PM UTC
Common questions about MYH10-related neurodevelopmental disorder with congenital anomalies
Patient case studies | 21 | 26% |
Research summaries | 16 | 20% |
Disease patterns and progression | 9 | 11% |
Other research | 5 | 6% |
Clinical study results | 4 | 5% |
Testing and diagnosis research | 1 | 1% |
Hutaff-Lee C (2026). [PMID: 40952039](https://pubmed.ncbi.nlm.nih.gov/40952039/). *Am J Med Genet A*. [Basic Science / Preclinical]
Xu D (2026). [PMID: 41232796](https://pubmed.ncbi.nlm.nih.gov/41232796/). *Exp Neurol*. [Case Report / Case Series]
Young RE (2026). [PMID: 40931319](https://pubmed.ncbi.nlm.nih.gov/40931319/). *Clin Genet*. [Case Report / Case Series]
Lee E (2026). [PMID: 41556401](https://pubmed.ncbi.nlm.nih.gov/41556401/). *Hum Mol Genet*. [Other]
Seed M (2026). [PMID: 42223939](https://pubmed.ncbi.nlm.nih.gov/42223939/). *JAMA Netw Open*. [Epidemiology / Natural History]
Maroni MJ (2026). [PMID: 40494548](https://pubmed.ncbi.nlm.nih.gov/40494548/). *Brain*. [Basic Science / Preclinical]
Chorin O (2025). [PMID: 40102980](https://pubmed.ncbi.nlm.nih.gov/40102980/). *Orphanet J Rare Dis*. [Case Report / Case Series]
Parkhill M (2025). [PMID: 40102109](https://pubmed.ncbi.nlm.nih.gov/40102109/). *Trends Pharmacol Sci*. [Review / Meta-Analysis]
Scheidecker S (2025). [PMID: 40044823](https://pubmed.ncbi.nlm.nih.gov/40044823/). *Eur J Hum Genet*. [Case Report / Case Series]
Fogelström A (2025). [PMID: 40983721](https://pubmed.ncbi.nlm.nih.gov/40983721/). *Pediatr Surg Int*. [Epidemiology / Natural History]