Cargando…
Severe neonatal hyperbilirubinemia secondary to combined RhC hemolytic disease, congenital hypothyroidism and large adrenal hematoma: a case report
BACKGROUND: ABO blood group incompatibility, neonatal sepsis, G-6-PD deficiency, thyroid dysfunction, and hereditary spherocytosis are all probable causes of neonatal hyperbilirubinemia. However, the etiology of some hyperbilirubinemia is extremely complicated, which may be caused by multiple factor...
Autores principales: | Dai, Chengiun, Chen, Chun, Jiang, Liqiong, Zhu, Yilin, Wang, Chunlin |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9465864/ https://www.ncbi.nlm.nih.gov/pubmed/36089589 http://dx.doi.org/10.1186/s12887-022-03594-7 |
Ejemplares similares
-
Physicochemical and Biological Characterization of rhC1INH Expressed in CHO Cells
por: Zubareva, Ekaterina, et al.
Publicado: (2021) -
Neonatal Adrenal Hemorrhage presenting as Prolonged Hyperbilirubinemia
por: Singh, Jasbir, et al.
Publicado: (2016) -
Congenital hypothyroidism in neonates
por: Anjum, Aneela, et al.
Publicado: (2014) -
Neonatal hyperbilirubinemia
por: Ben, Matteo Dal, et al.
Publicado: (2014) -
RhC Phenotyping, Adsorption/Elution Test, and SSP-PCR: The Combined Test for D-Elute Phenotype Screening in Thai RhD-Negative Blood Donors
por: Srijinda, Songsak, et al.
Publicado: (2012)