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...

Täydet tiedot

Tallennettuna:
Bibliografiset tiedot
Julkaisussa:Medicine (Baltimore)
Päätekijät: Portaro, Simona, Naro, Antonino, Guarneri, Claudio, Di Toro, Giuseppe, Manuli, Alfredo, Calabrò, Rocco Salvatore
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: Wolters Kluwer Health 2018
Aiheet:
Research Article
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC6283126/
https://ncbi.nlm.nih.gov/pubmed/30508964
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1097/MD.0000000000013448
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