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Trichodental syndrome is characterized by the association of fine, dry and short hair with dental anomalies. It has been described in less than 10 families. The mode of transmission is autosomal dominant.
Features include: Microcephaly, Fine hair, Odontodysplasia, and Brittle hair and 4 more.
Organ System | Phenotype Count | Example Features |
|---|---|---|
Head and neck | 1 | Microcephaly |
Biomarker and diagnostic research for trichodental syndrome has been reported in the published literature.
Estimated prevalence: <1 in 1,000,000 (VERY_RARE).
No clinical trials have been registered for trichodental syndrome.
3 publications have been identified in PubMed for trichodental syndrome. Kisho has analyzed 2 by research type. Research spans Diagnostic / Biomarker (100%).
Singh Y (2026). [PMID: 41944883](https://pubmed.ncbi.nlm.nih.gov/41944883/). *J Trauma Acute Care Surg*. [Diagnostic / Biomarker]
Cezar G (2024). [PMID: 39656698](https://pubmed.ncbi.nlm.nih.gov/39656698/). *PLoS One*. [Diagnostic / Biomarker]
Data assembled from 5 of 12 sources · Last updated Sep 19, 2026, 6:46 AM UTC
Online Mendelian Inheritance in Man
European rare disease database
Genetic and Rare Diseases Info Center