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Odontogenic myxofibroma of gingiva in a pediatric patient with tuberous sclerosis: A rare case report
Tuberous sclerosis complex (TSC) is a rare multisystem genetic disease, with an estimated incidence of 1 in 6000–1 in 10,000. TSC is an autosomal dominant syndrome involving heart, kidneys, lungs, and skin. The classic triad of TSC is seizures, mental retardation, and angiofibromas; this triad occur...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Medknow Publications & Media Pvt Ltd
2016
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5141676/ https://www.ncbi.nlm.nih.gov/pubmed/27994429 http://dx.doi.org/10.4103/0976-237X.194120 |