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Hemoglobin ; 36(2): 109-13, 2012.
Article in English | MEDLINE | ID: mdl-22384797

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 ß-globin gene is Hb Kansas [ß102(G4)Asn→Thr, AAC>ACC].


Subject(s)
Cyanosis/genetics , Fetal Hemoglobin/genetics , Oxygen/metabolism , Point Mutation , gamma-Globins/genetics , Base Sequence , Cyanosis/diagnosis , Cyanosis/metabolism , DNA Mutational Analysis , Female , Hemoglobins, Abnormal/genetics , Humans , Infant, Newborn , Molecular Sequence Data , Sequence Homology, Amino Acid
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