HB P-Nilotic or α₂(βδ)₂ in a Turkish Family

C. Altay Department of Pediatrics, Hacettepe University, Ankara, Turkey

A. Kutlar Department of Cell and Molecular Biology Laboratory of Protein Chemistry, Medical College of Georgia, Augusta, GA, 30912-3331, USA

J. B. Wilson Department of Cell and Molecular Biology Laboratory of Protein Chemistry, Medical College of Georgia, Augusta, GA, 30912-3331, USA

B. B. Webber Department of Cell and Molecular Biology Laboratory of Protein Chemistry, Medical College of Georgia, Augusta, GA, 30912-3331, USA

T. H.J. Huisman Department of Cell and Molecular Biology Laboratory of Protein Chemistry, Medical College of Georgia, Augusta, GA, 30912-3331, USA

Abstract

We recently examined a 16-year-old high school student who participated in a survey for Hemoglobinopathies in an Anatolian city in Turkey. Analysis if his hemoglobin (Hb) showed the presence of an electrophoretically slow-moving variant (at pH 8.6, about as Hb S) which, upon further examination, was also seen in his father, one brother, and one sister.

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HB P-Nilotic or α₂(βδ)₂ in a Turkish Family

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HB P-Nilotic or α₂(βδ)₂ in a Turkish Family