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X-linked sideroblastic anaemia in a female fetus: a case report and a literature review
BACKGROUND: X-linked sideroblastic anaemia (XLSA) is commonly due to mutations in the ALAS2 gene and predominantly affects hemizygous males. Heterozygous female carriers of the ALAS2 gene mutation are often asymptomatic or only mildly anaemic. XLSA is usually characterized by microcytic erythrocytes...
Autores principales: | Nzelu, Diane, Shangaris, Panicos, Story, Lisa, Smith, Frances, Piyasena, Chinthika, Alamelu, Jayanthi, Elmakky, Amira, Pelidis, Maria, Mayhew, Rachel, Sankaran, Srividhya |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8686580/ https://www.ncbi.nlm.nih.gov/pubmed/34930268 http://dx.doi.org/10.1186/s12920-021-01146-z |
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