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...

Ausführliche Beschreibung

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Bibliographische Detailangaben
Hauptverfasser: Canger, Emin Murat, Çelenk, Peruze, Devrim, İnci, Avşar, Aysun
Format: Artigo
Sprache:Inglês
Veröffentlicht: Hindawi Publishing Corporation 2013
Schlagworte:
Case Report
Online Zugang: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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