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Glassberg, J., Minnitti, C., Cromwell, C., Cytryn, L., Kraus, T., Skloot, G.S., et al. (2017) Inhaled Steroids Reduce Pain and Svcam Levels in Individuals with Sickle Cell Disease: A Triple‐Blind, Randomized Trial. American Journal of Hematology, 92, 622-631.
https://doi.org/10.1002/ajh.24742

has been cited by the following article:

• TITLE: Asthma Attack Revealing Sickle Cell Disease

  AUTHORS: Khaoula Achir, Ilham Tadmori, Moustapha Hida

  KEYWORDS: Sickle Cell Disease, Asthma, Morbidity

  JOURNAL NAME: Open Journal of Pediatrics, Vol.14 No.5, September 10, 2024

  ABSTRACT: Sickle cell disease is a genetic disorder characterized by the presence of hemoglobin S (HbS) and a significant reduction in normal hemoglobin A (HbA) in red blood cells. In deoxygenated conditions, HbS molecules polymerize, causing vascular occlusions and hemolysis. Pulmonary complications associated with this disease result from vascular occlusion, ischemia-reperfusion, and inflammation. Literature reports that asthma is observed in 30% to 70% of patients with sickle cell disease. We present the case of a boy whose sickle cell disease diagnosis was established following an asthma attack.