| Literature DB >> 19055867 |
Nazeer Alli1, Marius Coetzee, Vernon Louw, Ben van Rensburg, Gerrit Rossouw, Lisa Thompson, Serge Pissard, Swee Lay Thein.
Abstract
We report a case of sickle cell disease (SCD) in a patient who is a carrier for the sickle mutation with no additional mutations in the beta globin genes. Sequencing of the PK-LR genes showed that she was also heterozygous for the L272V mutation in exon 7, which is known to cause pyruvate kinase (PK) deficiency. It appeared that sickling in the heterozygous state is related to decreased oxygen affinity associated with PK deficiency in this unusual case.Entities:
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Year: 2008 PMID: 19055867 DOI: 10.1179/102453308X343536
Source DB: PubMed Journal: Hematology ISSN: 1024-5332 Impact factor: 2.269