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Hb J-Wenchang-Wuming [α11(A9)Lys→Gln (AAG>CAG) (α2 or α1)] compromises neonatal screening for α-thalassemia with the Sebia Capillarys2 electrophoresis system.
Zhai, Yin-Sheng; Tang, Hai-Shen; Li, Dong-Zhi.
Affiliation
  • Zhai YS; Department of Obstetrics and Gynecology, Nanlang Hospital of Zhongshan City, Zhongshan, Guangdong, People's Republic of China.
Hemoglobin ; 36(4): 395-8, 2012.
Article in En | MEDLINE | ID: mdl-22680346
We describe a Chinese newborn who was assumed to have α(0)-thalassemia (α(0)-thal) by determining the amount of Hb Bart's (γ4) in the cord blood, but was later shown to have only α(+)-thal. Hb J-Wenchang-Wuming [α11(A9)Lys→Gln (AAG>CAG) (α2 or α1)] was mistaken for Hb Bart's as both hemoglobin (Hb) variants have the same mobility.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Hemoglobins, Abnormal / Neonatal Screening / Alpha-Thalassemia / Electrophoresis, Capillary Type of study: Diagnostic_studies / Screening_studies Limits: Humans / Newborn Language: En Journal: Hemoglobin Year: 2012 Document type: Article Country of publication: United kingdom

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Hemoglobins, Abnormal / Neonatal Screening / Alpha-Thalassemia / Electrophoresis, Capillary Type of study: Diagnostic_studies / Screening_studies Limits: Humans / Newborn Language: En Journal: Hemoglobin Year: 2012 Document type: Article Country of publication: United kingdom