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Co-inheritance of haemoglobin A2' and beta-thalassaemia in cis.
Vermeersch, P; Philippe, M; Goossens, W.
Affiliation
  • Vermeersch P; Department of Laboratory Medicine, Hematology, University Hospitals Leuven, Catholic University of Leuven, Leuven, Belgium.
Int J Lab Hematol ; 30(4): 334-8, 2008 Aug.
Article in En | MEDLINE | ID: mdl-18665832
ABSTRACT
HbA2' is a haematologically silent delta chain variant that elutes in the S-region on high performance liquid chromatography. The major clinical significance of HbA2' is that failure to detect it might lead to failure to recognize beta-thalassaemia minor. Co-inheritance of HbA2' and beta-thalassaemia in cis has been described only once in a family from Suriname. We describe a new case of co-inheritance in cis of HbA2' and beta-thalassaemia in a family from Ghanaian origin with a HbA2' of more than 3%. Molecular investigation revealed the same mutations as in the family from Suriname, suggesting a common origin of both families.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Hemoglobin A2 / Beta-Thalassemia Limits: Adult / Child, preschool / Humans / Infant / Male Country/Region as subject: Africa Language: En Journal: Int J Lab Hematol Journal subject: HEMATOLOGIA Year: 2008 Document type: Article Affiliation country: Belgium

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Hemoglobin A2 / Beta-Thalassemia Limits: Adult / Child, preschool / Humans / Infant / Male Country/Region as subject: Africa Language: En Journal: Int J Lab Hematol Journal subject: HEMATOLOGIA Year: 2008 Document type: Article Affiliation country: Belgium