Oligodontia
Explore this rare clinical image of oligodontia—a genetic dental condition where six or more teeth are congenitally missing. Linked to PAX9, MSX1, and EDAR mutations.
oligodontia, tooth agenesis, congenital tooth loss, dental anomaly, PAX9 mutation, MSX1 gene, EDAR mutation, missing, permanent teeth, rare dental condition, non-syndromic oligodontia
This clinical photograph showcases oligodontia, a rare genetic condition characterized by the congenital absence of six or more permanent teeth. Often associated with PAX9, MSX1, or EDAR gene mutations, oligodontia is classified under non-syndromic tooth agenesis and affects less than 0.2% of the population.






ECTODERMAL DYSPLASIA
This is me. Living confidently with Ectodermal Dysplasia—raising awareness, building community, and breaking stigma. Let's normalize visible differences.
🔍 #EctodermalDysplasia #RareDiseaseAwareness #GeneticDisorders #HealthAdvocate #LivingWithED #DisabilityAwareness #InclusionMatters



