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Thorax ; 73(5): 489-492, 2018 05.
Artículo en Inglés | MEDLINE | ID: mdl-29382801

RESUMEN

Familial pulmonary fibrosis is associated with loss-of-function mutations in telomerase reverse transcriptase (TERT) and short telomeres. Interstitial lung diseases have become the leading indication for lung transplantation in the USA, and recent data indicate that pathogenic mutations in telomerase may cause unfavourable outcomes following lung transplantation. Although a rare occurrence, solid organ transplant recipients who develop acute graft-versus-host disease (GVHD) have very poor survival. This case report describes the detection of a novel mutation in TERT in a patient who had lung transplantation for familial pulmonary fibrosis and died from complications of acute GVHD.


Asunto(s)
Enfermedad Injerto contra Huésped/etiología , Trasplante de Pulmón/efectos adversos , Fibrosis Pulmonar/genética , Telomerasa/genética , Enfermedad Aguda , Resultado Fatal , Femenino , Enfermedad Injerto contra Huésped/patología , Humanos , Mutación , Fibrosis Pulmonar/cirugía , Telomerasa/metabolismo
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