Rothmund-Thomson Syndrome: A 13-Year Follow-Up

Rothmund-Thomson syndrome (RTS) is a rare autosomal recessive disorder presenting with poikiloderma and other clinical features, affecting the bones and eyes and, in type II RTS, presenting an increased risk for malignancy. With about 300 cases reported so far, we present a 13-year follow-up includi...

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Detalles Bibliográficos
Autores principales: Guerrero-González, Guillermo Antonio, Martínez-Cabriales, Sylvia Aideé, Hernández-Juárez, Aideé Alejandra, de Jesús Lugo-Trampe, José, Espinoza-González, Nelly Alejandra, Gómez-Flores, Minerva, Ocampo-Candiani, Jorge
Formato: Online Artículo Texto
Lenguaje:English
Publicado: S. Karger AG 2014
Materias:
Published online: July, 2014
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4127543/
https://www.ncbi.nlm.nih.gov/pubmed/25120469
http://dx.doi.org/10.1159/000365625

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4127543/
https://www.ncbi.nlm.nih.gov/pubmed/25120469
http://dx.doi.org/10.1159/000365625

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