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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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Autors principals: Canger, Emin Murat, Çelenk, Peruze, Devrim, İnci, Avşar, Aysun
Format: Artigo
Idioma:Inglês
Publicat: Hindawi Publishing Corporation 2013
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Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC3864084/
https://ncbi.nlm.nih.gov/pubmed/24363941
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1155/2013/935716
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