PREVALENCE OF ALPHA-THALASSEMIAS IN NORTHERN THAILAND

Citation
M. Lemmenszygulska et al., PREVALENCE OF ALPHA-THALASSEMIAS IN NORTHERN THAILAND, Human genetics, 98(3), 1996, pp. 345-347
Citations number
11
Categorie Soggetti
Genetics & Heredity
Journal title
ISSN journal
03406717
Volume
98
Issue
3
Year of publication
1996
Pages
345 - 347
Database
ISI
SICI code
0340-6717(1996)98:3<345:POAINT>2.0.ZU;2-3
Abstract
The population of northern Thailand has one of the highest frequencies of alpha-thalassemia in the world. However, the available distributio nal data are controversial. In addition to deletional types of alpha-t halassemia Hb, type Constant Spring should also be taken into consider ation in alpha-thalassemia population studies, because it causes clini cal alpha-thalassemia in the homozygous state or when present with bot h alpha-globin genes deleted in trans. We have examined a sample of 21 5 healthy subjects from four rural districts of Chiang Mai province. O ut of these, 77 exhibited anomalies of the alpha-globin genes (alpha a lpha/-alpha(3.7) in 36; -alpha(3.7)/-alpha(3.7) in 3; --(SEA) in 30; a lpha alpha/alpha(CS)alpha in 5; alpha alpha alpha(anti3.7) in 3). Ther efore, no fewer than 2% of the children in northern Thailand are expec ted to be born with HbH disease or thalassemic hydrops fetalis. The co nsiderable public health problem of hemoglobinopaties and the increasi ng acceptance of family planning necessitates facilities for the pre-a nd postnatal diagnosis of these disorders at the DNA level.