Cargando…
EIF2AK4 mutation in pulmonary veno-occlusive disease: A case report and review of the literature
BACKGROUND: Pulmonary veno-occlusive disease (PVOD) is a rare and devastating cause of pulmonary arterial hypertension with a non-specific clinical presentation and a relatively specific presentation in high-resolution thoracic CT scan images. Definitive diagnosis is made by histological examination...
Autores principales: | Liang, Li, Ma, Guofeng, Chen, Kai, Liu, Yangxiang, Wu, Xiaohong, Ying, Kejing, Zhang, Ruifeng |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Wolters Kluwer Health
2016
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5265969/ https://www.ncbi.nlm.nih.gov/pubmed/27684876 http://dx.doi.org/10.1097/MD.0000000000005030 |
Ejemplares similares
-
A rare compound heterozygous EIF2AK4 mutation in pulmonary veno-occlusive disease
por: Zhang, Chun, et al.
Publicado: (2022) -
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) -
Good response to PAH-targeted drugs in a PVOD patient carrying Biallelic EIF2AK4 mutation
por: Liang, Li, et al.
Publicado: (2018) -
Pulmonary spindle cell carcinoma with unusual morphology: A rare case report and review of the literature
por: Qi, Dian-Jun, et al.
Publicado: (2017) -
Pulmonary Langerhans Cell Histiocytosis: Case Series and Literature Review
por: Wei, Ping, et al.
Publicado: (2014)