Alpha thalassemia screenign in neonates by mean corpuscular volume and mean corpuscular hemoglobin determination

Alvin H. Schmaier, Harold M. Maurer, Charles L. Johnston, Robert B. Scott

Research output: Contribution to journalArticlepeer-review

29 Scopus citations

Abstract

Although alpha thalassemia trait may be diagnosed in the neonate by the presence of hemoglobin Barts, no simple screeing test for this disorder is available. This study was performed to determine whether the mean corpucular volume (MCV) and mean corpuscular hemoglobin (MCH) could serve this purpose. Capillary blood samples from 200 full-term black infants, 1 to 3 days of age, were drawn for electronic determination of red cell indices and hemoglobin electrophorssis on cellulose aetate. Of the 200 infants, 9 had MCV's of ≤94 μ3 and MCH's of ≤29.5 μμg, and of these, 6 (67 per cent) had hemoglobin Barts. No infant with hemoglobin Barts had an index in the normal range. We conclude that alpha thalassemia may be easily detected through MSCV and MCH screening of newborn populations at risk. An MCV ≤94 μ3 and an MCH <-29.5 μμg in the neonate is abnormal and should be followed by hemoglobin electrophoresis.

Original languageEnglish (US)
Pages (from-to)794-797
Number of pages4
JournalThe Journal of Pediatrics
Volume83
Issue number5
DOIs
StatePublished - Nov 1973

ASJC Scopus subject areas

  • Pediatrics, Perinatology, and Child Health

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