Cargando…
Pulmonary capillary hemangiomatosis: a focus on the EIF2AK4 mutation in onset and pathogenesis
Pulmonary capillary hemangiomatosis (PCH) is a pulmonary vascular disease that mainly affects small capillaries in the lung, and is often misdiagnosed as pulmonary arterial hypertension or pulmonary veno-occlusive disease due to similarities in their clinical presentations, prognosis, and management...
Autores principales: | Ma, Lijiang, Bao, Ruijun |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove Medical Press
2015
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4536836/ https://www.ncbi.nlm.nih.gov/pubmed/26300654 http://dx.doi.org/10.2147/TACG.S68635 |
Ejemplares similares
-
Novel EIF2AK4 mutations in histologically proven pulmonary capillary hemangiomatosis and hereditary pulmonary arterial hypertension
por: Abou Hassan, Ossama K., et al.
Publicado: (2019) -
Differential Diagnosis of Pulmonary Veno-Occlusive Disease and/or Pulmonary Capillary Hemangiomatosis after Identification of Two Novel EIF2AK4 Variants by Whole-Exome Sequencing
por: Park, Jong Eun, et al.
Publicado: (2023) -
Familial Pulmonary Capillary Hemangiomatosis Early in Life
por: Wirbelauer, Johannes, et al.
Publicado: (2011) -
Pulmonary capillary hemangiomatosis: a lesson learned
por: Guzman, Samuel, et al.
Publicado: (2019) -
Pulmonary capillary hemangiomatosis: an uncommon cause of pulmonary hypertension
por: Faria, Igor Murad, et al.
Publicado: (2013)