Molecular variations linked to the grouping of beta- and alpha-globin genes in neonatal patients with sickle cell disease in the State of Pernambuco, Brazil.

Abstract

Various factors have been described as phenotypic modulators of sickle cell disease, such as levels of fetal hemoglobin (Hb F), presence of alpha-thalassemia (thal), and haplotypes of the beta-globin genes. In order to characterize and determine the frequency of the betaS and betaC mutations and the prevalence of -alpha3.7-thal, 74 patients with sickle cell disease detected during neonatal screening in the State of Pernambuco, Brazil, were studied. The haplotypes of the beta gene and -alpha3.7-thal were determined using polymerase chain reaction (PCR), and specific restriction endonucleases were used to establish the polymorphic sites of the haplotypes. The results showed the high frequency of the Central African Republic (CAR) or Bantu haplotype in the State of Pernambuco, Brazil. The low frequency of the Benin haplotype recorded in this study, in comparison with other states in northeast Brazil, suggests the diversity of origins of Afro-Brazilians in this region.

• Authors: Marcos André C Bezerra, Magnun N N Santos, Aderson S Araújo, Yara M Gomes, Frederico G C Abath, Flavia M G C Bandeira
• Journal: Hemoglobin (Hemoglobin) Vol. 31 Issue 1 Pg. 83-8 ( 2007) ISSN: 0363-0269 [Print] England
• PMID: 17365008 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)

Chemical References

• Hemoglobin, Sickle
• Globins

Topics

• Anemia, Sickle Cell (blood, ethnology, genetics)
• Black People (ethnology, genetics)
• Brazil (ethnology)
• Child, Preschool
• Female
• Globins (genetics)
• Haplotypes (genetics)
• Hemoglobin, Sickle (genetics)
• Humans
• Infant
• Male
• alpha-Thalassemia (ethnology, genetics)
• beta-Thalassemia (ethnology, genetics)