Parin Kamseng1, Satariya Trakulsrichai2,3, Objoon Trachoo4,5, Walaiporn Yimniam1, Bhakbhoom Panthan1,5, Paisan Jittorntam6, Pimjai Niparuck4, Pitsucha Sanguanwit2, Winai Wananukul3,4, Sumalee Jindadamrongwech1. 1. a Department of Pathology, Faculty of Medicine , Ramathibodi Hospital, Mahidol University , Bangkok , Thailand. 2. b Department of Emergency Medicine, Faculty of Medicine , Ramathibodi Hospital, Mahidol University , Bangkok , Thailand. 3. c Ramathibodi Poison Center, Faculty of Medicine , Ramathibodi Hospital, Mahidol University , Bangkok , Thailand. 4. d Department of Medicine, Faculty of Medicine , Ramathibodi Hospital, Mahidol University , Bangkok , Thailand. 5. e Medical Genomic Center, Faculty of Medicine , Ramathibodi Hospital, Mahidol University , Bangkok , Thailand. 6. f Ramathibodi Research Center, Faculty of Medicine , Ramathibodi Hospital, Mahidol University , Bangkok , Thailand.
Abstract
OBJECTIVE: To investigate the cause(s) of a Thai male proband presenting low oxygen saturation by pulse oximetry (SpO2) and severe anemia. METHODS: As Hb variant was suspected, Hb typing was determined by high-performance liquid chromatography and capillary electrophoresis, and subsequently Hb variant was identified by DNA sequencing. Complete blood counts were performed using automated blood cell counter and oxygen saturation was measured by pulse oximetry. RESULTS: Proband was compound heterozygous for Hb Louisville [β42(CD1)Phe→Leu] and Hb La Desirade [β129(H7)Ala→Val]. Of the proband's two sons, one was compound heterozygous for Hb Louisville and Hb E and the other for Hb La Desirade and Hb E. The former son had similar clinical features and laboratory findings with those of the proband while the latter showed had no abnormal clinical manifestations. CONCLUSION: This the first report of compound heterozygosity of Hb Louisville and Hb La Desirade in an individual of Southeast Asian ethnicity. Hb variant identification is crucial for genetic counseling and appropriate treatment in regions where hemoglobinopathies are common.
OBJECTIVE: To investigate the cause(s) of a Thai male proband presenting low oxygen saturation by pulse oximetry (SpO2) and severe anemia. METHODS: As Hb variant was suspected, Hb typing was determined by high-performance liquid chromatography and capillary electrophoresis, and subsequently Hb variant was identified by DNA sequencing. Complete blood counts were performed using automated blood cell counter and oxygen saturation was measured by pulse oximetry. RESULTS: Proband was compound heterozygous for Hb Louisville [β42(CD1)Phe→Leu] and Hb La Desirade [β129(H7)Ala→Val]. Of the proband's two sons, one was compound heterozygous for Hb Louisville and Hb E and the other for Hb La Desirade and Hb E. The former son had similar clinical features and laboratory findings with those of the proband while the latter showed had no abnormal clinical manifestations. CONCLUSION: This the first report of compound heterozygosity of Hb Louisville and Hb La Desirade in an individual of Southeast Asian ethnicity. Hb variant identification is crucial for genetic counseling and appropriate treatment in regions where hemoglobinopathies are common.
Authors: S Alkindi; S Al Zadjali; M Al Rawahi; H Al Haddabi; S Daar; R A ElSadek; B D Sherkawy; A V Pathare Journal: Mediterr J Hematol Infect Dis Date: 2021-01-01 Impact factor: 2.576