Common Somatic Alterations Identified in Maffucci Syndrome by Molecular Karyotyping

Maffucci syndrome (MS) is a rare congenital disorder characterized by multiple central cartilaginous tumors (enchondromas) in association with cutaneous spindle cell hemangiomas. These patients have a high incidence of malignant transformation. No familial case is known and the etiopathogenic cause...

Popoln opis

Shranjeno v:
Bibliografske podrobnosti
izdano v:Mol Syndromol
Main Authors: Amyere, Mustapha, Dompmartin, Anne, Wouters, Vinciane, Enjolras, Odile, Kaitila, Ilkka, Docquier, Pierre-Louis, Godfraind, Catherine, Mulliken, John Butler, Boon, Laurence Myriam, Vikkula, Miikka
Format: Artigo
Jezik:Inglês
Izdano: S. Karger AG 2014
Teme:
Original Article
Online dostop:https://ncbi.nlm.nih.gov/pmc/articles/PMC4281579/
https://ncbi.nlm.nih.gov/pubmed/25565925
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1159/000365898
Oznake: Označite
Brez oznak, prvi označite!

Podobne knjige/članki