Hemangiomas of the tongue and the oral cavity in a myotonic dystrophy type 1 patient: A case report

RATIONALE: Myotonic dystrophy type 1 (DM1) is an autosomal dominant disease caused by a cytosine, guanine, thymine (CTG) trinucleotide repeat expansion in the non-coding region of dystrophia myotonica protein kinase gene, causing a multisystem involvement. To date, few studies have been performed to...

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Detalles Bibliográficos
Autores principales: Portaro, Simona, Naro, Antonino, Guarneri, Claudio, Di Toro, Giuseppe, Manuli, Alfredo, Calabrò, Rocco Salvatore
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer Health 2018
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6283126/
https://www.ncbi.nlm.nih.gov/pubmed/30508964
http://dx.doi.org/10.1097/MD.0000000000013448

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6283126/
https://www.ncbi.nlm.nih.gov/pubmed/30508964
http://dx.doi.org/10.1097/MD.0000000000013448

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