| Autor: |
de Araújo MC; Departamento de Pediatria, Universidade Federal do Rio Grande do Norte, Natal, RN, Brasil. cristinapignataro@bol.com.br, Serafim ES, de Castro WA Jr, de Medeiros TM |
| Jazyk: |
portugalština |
| Zdroj: |
Cadernos de saude publica [Cad Saude Publica] 2004 Jan-Feb; Vol. 20 (1), pp. 123-8. Date of Electronic Publication: 2004 Mar 08. |
| DOI: |
10.1590/s0102-311x2004000100027 |
| Abstrakt: |
Hemoglobinopathies are among the most prevalent hereditary diseases in humans. Studies in different areas of Brazil have identified the prevalence of S and C abnormal hemoglobins. The study analyzed 1,940 cord blood samples of newborns from maternity hospitals in Natal, Rio Grande do Norte State, to investigate the prevalence of abnormal hemoglobins. All samples were submitted to cellulose acetate electrophoresis using a Tris-EDTA-borate buffer at pH 8.5. Electrophoresis in agar gel pH 6.2 was performed on samples presenting abnormal hemoglobin. Some 37 (1.91%) of the newborns presented hemoglobinopathies, as follows: 29 (1.50%) sickle cell trait (Hb FAS), 6 (0.31%) heterozygous Hb C (Hb FAC), one (0.05%) homozygous Hb S (Hb FS), and one (0.05%) Hb Barts suggestive of alpha thalassemia. The results show the need to implement screening for hemoglobinopathies in the neonatal population. |
| Databáze: |
MEDLINE |
| Externí odkaz: |
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