Newborn diagnosis of abnormal hemoglobins from a large municipal hospital in Los Angeles.
Author(s) -
Nadia P. Ewing,
D Powars,
J Hilburn,
Werner Schroeder
Publication year - 1981
Publication title -
american journal of public health
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.284
H-Index - 264
eISSN - 1541-0048
pISSN - 0090-0036
DOI - 10.2105/ajph.71.6.629
Subject(s) - sickle cell trait , medicine , sickle cell anemia , pediatrics , hemoglobinopathy , anemia , newborn screening , hemoglobin s , hemoglobin , disease , hemoglobin c , cord blood , trait , computer science , programming language
Cord blood samples from 29,611 infants born in Los Angeles over a 71/2 year period were examined for hemoglobinopathies. Among 4,134 Black newborns, the frequency of sickle cell anemia (SS) was 0.3 per cent, of sickle cell trait (AS) 8 per cent, and of Hb-C trait (AC) 2 per cent. Of 17,781 Spanish surnamed (Mexican) newborns, 0.5 per cent had sickle cell trait, and 0.1 per cent had Hb-C trait. Of the 5,541 Caucasian infants, 0.7 per cent had sickle cell trait, and 0.15 per cent had Hb-C trait. Twenty-three Black children with major hemoglobinopathies included 16 with sickle cell anemia, two with hemoglobin C disease (CC), and five with SC disease.
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