X-linked sideroblastic anaemia in a female fetus: a case report and a literature review
Abstract 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 eryt...
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| Main Authors: | , , , , , , , , , |
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| Format: | Book |
| Published: |
BMC,
2021-12-01T00:00:00Z.
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