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|Title:||Alpha-thalassemia in a selected population of Mexico|
|Abstract:||Objective. To identify by molecular biology the alleles of α-Thal in selected hospital populations. Methods. Eighteen propositi with hematological and biochemical data suggestive of α-thalassemia, selected from 356 patients of four hospitals in two cities with probable hemoglobinopathy were investigated for six common α-Thal alleles. Molecular studies were done by PCR and digestion with specific restriction enzymes. Results. The α 3.7 allele was identified in two cases and the family study revealed the same allele in the mother; HbS heterozigocity was also detected in one of them. An analysis with Apa I demonstrated a class I deletion in both patients. The present study showed 2/356 (0.6%) of α 3.71 carriers which is a low frequency as compared with other countries. As no other common α-thalassemia alleles were found, we suspect that α-Thal in Mexico is as heterogeneous at a molecular level as β-Thal.|
|Appears in Collections:||Producción científica UdeG (prueba)|
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