Cargando…
Case of Congenital Hemolytic Anemia with ATP11C and ANK1 Variants
A male infant of Han descent, with a G(1)P(1) mother and gestational age of 40(+4) weeks, was born via cesarean section owing to his mother having pregnancy complications, including premature rupture of membranes, chorioamnionitis, and gestational diabetes. On the first day after birth, routine bloo...
Autores principales: | Xu, Wei, Ma, Mengmeng, Zhao, Sai, Yuan, Yufang, Tian, Zhaofang |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2023
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10605443/ https://www.ncbi.nlm.nih.gov/pubmed/37892263 http://dx.doi.org/10.3390/children10101600 |
Ejemplares similares
-
Exome sequencing for diagnosis of congenital hemolytic anemia
por: Mansour-Hendili, Lamisse, et al.
Publicado: (2020) -
Congenital Hemolytic Anemias: Is There a Role for the Immune System?
por: Zaninoni, Anna, et al.
Publicado: (2020) -
A Rare Variant of ANK3 Is Associated With Intracranial Aneurysm
por: Liu, Junyu, et al.
Publicado: (2021) -
Autoimmune Hemolytic Anemia as a Complication of Congenital Anemias. A Case Series and Review of the Literature
por: Motta, Irene, et al.
Publicado: (2021) -
Confounding factors in the diagnosis and clinical course of rare congenital hemolytic anemias
por: Fattizzo, Bruno, et al.
Publicado: (2021)