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An instance of narcolepsy that is caused by an inherited genomic modification in an individual.
No clinical trials have been registered for hereditary narcolepsy.
5 publications have been identified in PubMed for hereditary narcolepsy. Research spans Case Report / Case Series (60%) and Review / Meta-Analysis (40%).
Park YA (2025). [PMID: 41445556](https://pubmed.ncbi.nlm.nih.gov/41445556/). *JBMR Plus*. [Review / Meta-Analysis]
Osundiji MA (2025). [PMID: 41165919](https://pubmed.ncbi.nlm.nih.gov/41165919/). *Chromosome Res*. [Case Report / Case Series]
Tamura M (2025). [PMID: 40937613](https://pubmed.ncbi.nlm.nih.gov/40937613/). *Neurocase*. [Case Report / Case Series]
Unoki M (2025). [PMID: 40500184](https://pubmed.ncbi.nlm.nih.gov/40500184/). *Genes Genet Syst*. [Review / Meta-Analysis]
Mizuno Y (2024). [PMID: 37984842](https://pubmed.ncbi.nlm.nih.gov/37984842/). *J Sleep Res*. [Case Report / Case Series]
Data assembled from 2 of 12 sources · Last updated Sep 18, 2026, 7:12 PM UTC