Hb J-Wenchang-Wuming [α11(A9)LysâGln (AAG>CAG) (α2 or α1)] compromises neonatal screening for α-thalassemia with the Sebia Capillarys2 electrophoresis system.
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)LysâGln (AAG>CAG) (α2 or α1)] was mistaken for Hb Bart's as both hemoglobin (Hb) variants have the same mobility.
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