| Literature DB >> 22384797 |
Urs Zimmermann-Baer1, Ralph Capalo, Fabrizio Dutly, Elisabeth Saller, Heinz Troxler, Malcolm Kohler, Hannes Frischknecht.
Abstract
A baby girl, born at term, presented with severe cyanosis and received oxygen supplementation. Consecutive arterial blood gas analysis showed a pronounced right shift of the saturation curve, suggesting the presence of a hemoglobin (Hb) variant. A new (G)γ-globin variant was detected, namely HBG2:c.308G, which we have named Hb F-Sarajevo, the city from where the baby's parents originate. This A to C transversion exists in cis to the common (A)γ(T) and the resulting mutant Hb molecule exhibits very low oxygen affinity and cooperativity. Its analogue in the β-globin gene is Hb Kansas [β102(G4)Asn→Thr, AAC>ACC].Entities:
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Year: 2012 PMID: 22384797 DOI: 10.3109/03630269.2012.655872
Source DB: PubMed Journal: Hemoglobin ISSN: 0363-0269 Impact factor: 0.849