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No clinical trials have been registered for isolated congenital hypoglossia.
7 publications have been identified in PubMed for isolated congenital hypoglossia. Research spans Case Report / Case Series (57%), Epidemiology / Natural History (29%), and Review / Meta-Analysis (14%).
Velisavljev-Filipovic GM (2025). [PMID: 40709982](https://pubmed.ncbi.nlm.nih.gov/40709982/). *Diseases*. [Case Report / Case Series]
Augustyniak A (2025). [PMID: 39913022](https://pubmed.ncbi.nlm.nih.gov/39913022/). *Vet Res Commun*. [Epidemiology / Natural History]
Al-Bdairi FJ (2025). [PMID: 40557005](https://pubmed.ncbi.nlm.nih.gov/40557005/). *Cureus*. [Case Report / Case Series]
Webb BD (2025). [PMID: 40662098](https://pubmed.ncbi.nlm.nih.gov/40662098/). *Genet Med Open*. [Review / Meta-Analysis]
Jha M (2024). [PMID: 39822794](https://pubmed.ncbi.nlm.nih.gov/39822794/). *J Clin Exp Dent*. [Case Report / Case Series]
Jabbari J (2024). [PMID: 38940227](https://pubmed.ncbi.nlm.nih.gov/38940227/). *Vet Med Sci*. [Epidemiology / Natural History]
Al Hariri B (2024). [PMID: 38764739](https://pubmed.ncbi.nlm.nih.gov/38764739/). *J Surg Case Rep*. [Case Report / Case Series]
Data assembled from 3 of 12 sources · Last updated Sep 18, 2026, 7:14 PM UTC
European rare disease database
Genetic and Rare Diseases Info Center
AI-curated news mentioning isolated congenital hypoglossia
Updated Feb 10, 2024
A case report details Oromandibular Limb Hypogenesis Syndrome Type IVB, highlighting its association with hypoglossia and intraoral bands. This rare entity contributes to the understanding of congenital anomalies and their clinical implications.