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Systemic mastocytosis with KIT V560G mutation presenting as recurrent episodes of vascular collapse: response to disodium cromoglycate and disease outcome
BACKGROUND: Mastocytosis are rare diseases characterized by an accumulation of clonal mast cells (MCs) in one or multiple organs or tissues. Patients with systemic mastocytosis (SM), whose MCs frequently arbor the activating D816V KIT mutation, may have indolent to aggressive diseases, and they may...
Autores principales: | Conde-Fernandes, Iolanda, Sampaio, Rita, Moreno, Filipa, Palla-Garcia, José, Teixeira, Maria dos Anjos, Freitas, Inês, Neves, Esmeralda, Jara-Acevedo, Maria, Escribano, Luis, Lima, Margarida |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5402055/ https://www.ncbi.nlm.nih.gov/pubmed/28439288 http://dx.doi.org/10.1186/s13223-017-0193-x |
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