Cargando…
Incidentally detected asplenia in a healthy 64-year-old female live kidney donor
Heterotaxia syndromes are rare birth defects which can result in developmental malformations. A 64-year-old woman presented to the hospital for preoperative screening for kidney donation; during which she was found to have no gallbladder and no spleen, without any signs of surgical removal. This cou...
Autores principales: | Wolff, Leoniek D., Nijboer, Mijntje N., vd Wetering, Jacqueline, Dor, Frank J.M.F. |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2017
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5410883/ https://www.ncbi.nlm.nih.gov/pubmed/28473921 http://dx.doi.org/10.1093/omcr/omx012 |
Ejemplares similares
-
Isolated congenital asplenia: An overlooked cause of thrombocytosis
por: Borsani, Oscar, et al.
Publicado: (2022) -
ZEB2, a new candidate gene for asplenia
por: Pons, Linda, et al.
Publicado: (2014) -
Campylobacter jejuni bacteremia in a patient with asplenia and enteritis
por: Isabel, Ramírez
Publicado: (2019) -
COVID-19 and asplenia: a Janus-faced issue
por: Lenti, Marco Vincenzo, et al.
Publicado: (2021) -
The Effect of Donors’ Demographic Characteristics in Renal Function Post-Living Kidney Donation. Analysis of a UK Single Centre Cohort
por: Bellini, Maria Irene, et al.
Publicado: (2019)