2019
DOI: 10.1002/mgg3.795
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Incidence, demographic characteristics, and geographic distribution of sickle cell trait and sickle cell anemia births in Michigan, 1997–2014

Abstract: Background This study describes the incidence, demographic characteristics, and geographic distribution of sickle cell anemia (SCA) and sickle cell trait births in Michigan. Methods Michigan newborn screening records and birth certificates (1997–2014) were used to identify sickle cell trait and SCA births, as well as demographic characteristics and mother's residential address. Incidence was calculated overall and by county. Results During the study period, there were 592 SCA births and 33,404 sickle cell trai… Show more

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Cited by 15 publications
(9 citation statements)
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References 32 publications
(58 reference statements)
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“…A large majority of patients with SCD were African American whereas the non‐SCD group was predominantly Hispanic and Caucasian, an expected demographic finding as African American patients are more affected by SCD 19 . African American patients have also been shown to be at increased risk of OSA 20 .…”
Section: Discussionmentioning
confidence: 95%
“…A large majority of patients with SCD were African American whereas the non‐SCD group was predominantly Hispanic and Caucasian, an expected demographic finding as African American patients are more affected by SCD 19 . African American patients have also been shown to be at increased risk of OSA 20 .…”
Section: Discussionmentioning
confidence: 95%
“…The incidence of new diagnosis of sickle cell anemia is the highest in the State of Michigan within the city of Detroit, at 12.4 per 10,000 live births recorded in 2014. Sickle cell trait was diagnosed in Detroit in 581.4 per 10,000 births [3].…”
Section: Case Sex Age Genotype Bmi Kg/m2 Sickle Cell Complications Imentioning
confidence: 99%
“…Sickle cell disease, the most common hemoglobinopathy in the world, affects an estimated 100,000 Americans, 1 with an additional three million Americans carrying the trait. 2 The pathophysiology of the disease involves a point mutation in the beta globin gene, which results in the substitution of glutamic acid for valine. 3 In homozygotes (HbSS), the abnormal hemoglobin molecules polymerize and red blood cells subsequently form rigid, crescent shaped structures that are prone to causing vaso-occlusive events and downstream hypoxia.…”
Section: Introductionmentioning
confidence: 99%