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Noneruption of teeth - maxillary hypoplasia - genu valgum is an extremely rare syndrome that is characterized by multiple unerupted permanent teeth, hypoplasia of the alveolar process and of the maxillo-zygomatic region, severe genu valgum and deformed ears.
Estimated prevalence: <1 in 1,000,000 (VERY_RARE).
No clinical trials have been registered for non-eruption of teeth-maxillary hypoplasia-genu valgum syndrome.
2 publications have been identified in PubMed for non-eruption of teeth-maxillary hypoplasia-genu valgum syndrome. Research spans Review / Meta-Analysis (100%).
Al Ojaimi M (2025). [PMID: 40301961](https://pubmed.ncbi.nlm.nih.gov/40301961/). *Hum Genomics*. [Review / Meta-Analysis]
Gravholt CH (2024). [PMID: 38748847](https://pubmed.ncbi.nlm.nih.gov/38748847/). *Eur J Endocrinol*. [Review / Meta-Analysis]
Data assembled from 4 of 12 sources · Last updated Sep 20, 2026, 9:50 PM UTC
Online Mendelian Inheritance in Man
European rare disease database
Genetic and Rare Diseases Info Center