Cargando…
Atypical hereditary spherocytosis phenotype associated with pseudohypokalaemia and a new variant in the band 3 protein
Red blood cell (RBC) membrane disorders are predominantly caused by mutations resulting in decreased RBC deformability and permeability. We present a family in which, the proband and his daughter presented with pseudohypokalaemia. Studies on the temperature dependence of pseudohypokalaemia suggested...
Autor principal: | Ramasamy, Indra |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BMJ Publishing Group
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7733106/ https://www.ncbi.nlm.nih.gov/pubmed/33298499 http://dx.doi.org/10.1136/bcr-2020-238428 |
Ejemplares similares
-
Hereditary Spherocytosis as an Atypical Presentation of Anemia in Ulcerative Colitis
por: Cho, Moo, et al.
Publicado: (2021) -
Hereditary Spherocytosis
por: Huq, Sayeeda, et al.
Publicado: (2010) -
The Complexity of Genotype-Phenotype Correlations in Hereditary Spherocytosis: A Cohort of 95 Patients: Genotype-Phenotype Correlation in Hereditary Spherocytosis
por: van Vuren, Annelies, et al.
Publicado: (2019) -
Extramedullary paraspinal hematopoiesis in hereditary spherocytosis
por: Gogia, P., et al.
Publicado: (2008) -
Paravertebral pseudotumor in patient with hereditary spherocytosis
por: Rabelo, Lêda Maria, et al.
Publicado: (2016)