Hereditary nonspherocytic hemolytic anemia caused by glucose-6-phosphate isomerase (GPI) deficiency in a Chinese patient: a case report

BACKGROUND: Glucose phosphate isomerase (GPI) deficiency is a rare autosomal recessive disorder that causes hereditary nonspherocytic hemolytic anemia (HNSHA). Homozygous or compound heterozygous mutation of the GPI gene on chromosome 19q13 is the cause of GPI deficiency. Fifty-seven GPI mutations h...

Descripción completa

Detalles Bibliográficos
Autores principales: Zu, Yumei, Wang, Hui, Lin, Weijia, Zou, Chaochun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9341102/
https://www.ncbi.nlm.nih.gov/pubmed/35915427
http://dx.doi.org/10.1186/s12887-022-03522-9

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9341102/
https://www.ncbi.nlm.nih.gov/pubmed/35915427
http://dx.doi.org/10.1186/s12887-022-03522-9

Ejemplares similares