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J Pediatr Hematol Oncol ; 24(6): 499-502, 2002.
Article in English | MEDLINE | ID: mdl-12218602

ABSTRACT

Newborn screening for hemoglobinopathies rarely produces a fetal hemoglobin only result; it is most consistent with beta-thalassemia major, although other diagnoses are possible. The authors describe two unrelated African-American babies born in North Carolina whose newborn screening revealed fetal hemoglobin only. Both had a relatively benign clinical and hematologic picture. Molecular analyses indicated that both children are compound heterozygotes for beta-thalassemia and pancellular (deletional) hereditary persistence of fetal hemoglobin, a rare and apparently benign condition. Accurate interpretation of the fetal hemoglobin only result on newborn screening requires thorough evaluation, including family studies and molecular analysis.


Subject(s)
Fetal Hemoglobin/analysis , Hemoglobinopathies/diagnosis , Neonatal Screening , beta-Thalassemia/diagnosis , Black or African American , Female , Genetic Carrier Screening , Hematologic Tests , Hemoglobinopathies/blood , Hemoglobinopathies/genetics , Humans , Infant, Newborn , Male , Phenotype , beta-Thalassemia/blood , beta-Thalassemia/genetics
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