Severe Microcytic Anemia Caused by Complex Hereditary Spherocytosis and X-Linked Sideroblastic Anemia with Mutations in SPTB and ALAS2 Genes

We report a case of severe anemia caused by complex hereditary spherocytosis (HS) and X-linked sideroblastic anemia (XLSA) with two mutations in the spectrin beta (SPTB) and 5-aminolevulinic acid synthase (ALAS2) genes. The proband was a 16-year-old male with severe jaundice and microcytic hypochrom...

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Detalles Bibliográficos
Autores principales: Zhou, Jianying, Zhang, Hang, Qin, Yao, Liu, Ting
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10004689/
https://www.ncbi.nlm.nih.gov/pubmed/36902777
http://dx.doi.org/10.3390/jcm12051990

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10004689/
https://www.ncbi.nlm.nih.gov/pubmed/36902777
http://dx.doi.org/10.3390/jcm12051990

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