Article

Sickle cell, thalassemia, and heat: risk estimates and equity policy considerations from an exploratory timeseries study in California

2024-10-16

Abstract excerpt

<h4>ABSTRACT</h4> <h4>Background</h4> People born with hemoglobinopathies, such as sickle cell disease (SCD) and thalassemia, as well as people who are carriers for these disorders [sickle cell trait (SCT), thalassemia trait or thalassemia minor (TM)], may experience increased symptom-triggers and related illnesses from heat because their cells are susceptible to dehydration. Additionally, historical, and structur...

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Literature Corpus work: 7a650a88-e37e-557b-a55a-5c7d440e0ade
DOI: 10.1101/2024.10.15.24315547

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