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 includ...

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Bibliographic Details
Main Authors: Guerrero González, Guillermo Antonio, Martínez Cabriales, Sylvia Aideé, Hernández Juárez, Aideé Alejandra, Lugo Trampe, José de Jesús, Espinoza González, Nelly Alejandra, Gómez Flores, Minerva, Ocampo Candiani, Jorge
Format: Article
Language:English
Published: 2014
Subjects:
Online Access:http://eprints.uanl.mx/15236/1/338.pdf