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[Prevention of mediterranean anemia in Latium: Ida Bianco archives].

Medicina nei secoli - 1 Jan 2006

Falchetti Mario, Lupi Ramona, Ottini Laura

Abstract excerpt

Mediterranean anemia or beta-thalassemia is a hereditary syndrome characterized by a severe defect in haemoglobin production and an altered morphology of red blood cells. Homozygous condition for beta-thalassemia is characterized by short survival. Heterozygous condition is clinically found in ad...

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PMID: 17526287

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-17526287-2026-09-02.2. Manifest publication-graph-cohort-2026-09-02.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 2 Sept 2026.

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