Oral Findings of Rothmund-Thomson Syndrome

Rothmund-Thomson syndrome (RTS) is an extremely rare genetic condition exhibiting some dermatological, craniofacial, ophthalmological, and central nervous system abnormalities. It has an autosomal, recessive inheritance and its signs begin at childhood. Essential dermatological alteration is poikilo...

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Detalles Bibliográficos
Autores principales: Canger, Emin Murat, Çelenk, Peruze, Devrim, İnci, Avşar, Aysun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2013
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3864084/
https://www.ncbi.nlm.nih.gov/pubmed/24363941
http://dx.doi.org/10.1155/2013/935716

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3864084/
https://www.ncbi.nlm.nih.gov/pubmed/24363941
http://dx.doi.org/10.1155/2013/935716

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