The authors present 2 unusual cases of haemoglobin (Hb) Bart's hydrops fetalis and highlight the problem of a screening system for α-thalassaemia which focuses on maternal and paternal mean corpuscular volume (MCV) alone. Normal paternal MCV may not preclude fetal Hb Bart's disease because of the rare occurrence of maternal uniparental disomy or non-paternity. During a mid-trimester anomaly scan, with fetal cardiomegaly or hydrops in a woman with low MCV but normal paternal MCV, obstetricians should remain alert for fetal Hb Bart's disease. This is very important and relevant for national screening systems in South-East Asia, where a routine mid-trimester scan may not be available. A routine mid-trimester anomaly scan should therefore be implemented and in high prevalence areas, sonographers should be sensitive to the cardio-thoracic ratio even if screening shows that pregnancy is unlikely to be at risk.

1.
Liang ST, Wong V, So WK, Ma HK, Chan V, Todd: Homozygous α-thalassemia: clinical presentation, diagnosis and management. A review of 46 cases. Br J Obstet Gynaecol 1985;92:680-684.
2.
Leung KY, Lee CP, Tang MH, Lau ET, Ng LK, Lee YP, Chan HY, Ma ES, Chan V: Cost-effectiveness of prenatal screening for thalassaemia in Hong Kong. Prenat Diagn 2004;24:899-907.
3.
Chong SS, Boehm CD, Higgs DR, Cutting GR: Single-tube multiplex-PCR screen for common deletional determinants of α-thalassemia. Blood 2000;95:360-362.
4.
Lau ET, Tang L, Wong C, Lam YH, Ghosh A, Leung WC, Sin WK, Lau TK, Kung YY, Tang MH: Assessing discrepant findings between QF-PCR on uncultured prenatal samples and karyotyping on long-term culture. Prenat Diagn 2009;29:151-155.
5.
Wattanasirichaigoon D, Promsonthi P, Chuansumrit A, Leopairut J, Yanatatsaneejit P, Rattanatanyong P, Munkongdee T, Fucharoen S, Mutirangura A: Maternal uniparental disomy of chromosome 16 resulting in hemoglobin Bart's hydrops fetalis. Clin Genet 2008;74:284-287.
6.
Beldjord C, Henry I, Bennani C, Vanhaeke D, Labie D: Uniparental disomy: a novel mechanism for thalassemia major. Blood 1992;80:287-289.
7.
Kwan WY, So CH, Chan WP, Leung WC, Chow KM: Re-emergence of late presentations of fetal haemoglobin Bart's disease in Hong. Hong Kong Med J 2011;17:434-440.
8.
Li D, Liao C: Incidental discovery of nonpaternity during prenatal testing of genetic disease. Fetal Diagn Ther 2008;24:39-41.
9.
Hromadnikova I, Vechetova L, Vesela K, Benesova B, Doucha J, Kulovany E, Vlk R: Non-invasive fetal RHD exon 7 and exon 10 genotyping using real-time PCR testing of fetal DNA in maternal plasma. Fetal Diagn Ther 2005;20:275-280.
10.
Ma ESK, Chan AYY, Ha SY, Lau YL, Chan LC: Thalassaemia screening based on red cell indices in the Chinese. Haematologica 2001;86:1286-1287.
11.
Chui DH, Waye JS: Hydrops fetalis caused by α-thalassemia: an emerging healthcare problem. Blood 1998;91:2213-2222.
12.
Sirichotiyakul S, Maneerat J, Sanguansermsri T, Dhananjayanonda P, Tongsong T: Sensitivity and specificity of mean corpuscular volume testing for screening for α-thalassemia-1 and β-thalassemia traits. J Obstet Gynaecol Res 2005;31:198-201.
13.
Leung KY, Liao C, Li QM, Ma SY, Tang MH, Lee CP, Chan V, Lam YH: A new strategy for prenatal diagnosis of homozygous α0-thalassemia. Ultrasound Obstet Gynecol 2006;28:173-177.
14.
Vichinsky E: Complexity of α-thalassemia: growing health problem with new approaches to screening, diagnosis, and therapy. Ann NY Acad Sci 2010;1202:180-187.
15.
Salomon LJ, Alfirevic Z, Berghella V, Bilardo C, Hernandez-Andrade E, Johnsen SL, Kalache K, Leung KY, Malinger G, Munoz H, Prefumo F, Toi A, Lee W: ISUOG Clinical Standards Committee: Practice guidelines for performance of the routine mid-trimester fetal ultrasound scan. Ultrasound Obstet Gynecol 2011;37:116-126.
16.
Lau YL, Chan LC, Chan AYY, Hu SY, Yeung CY, Waye JS, Chui DHK: Prevalence and genotypes of α- and β-thalassemia carriers in Hong Kong - implications for population screening. N Engl J Med 1997;336:1298-1301.
Copyright / Drug Dosage / Disclaimer
Copyright: All rights reserved. No part of this publication may be translated into other languages, reproduced or utilized in any form or by any means, electronic or mechanical, including photocopying, recording, microcopying, or by any information storage and retrieval system, without permission in writing from the publisher.
Drug Dosage: The authors and the publisher have exerted every effort to ensure that drug selection and dosage set forth in this text are in accord with current recommendations and practice at the time of publication. However, in view of ongoing research, changes in government regulations, and the constant flow of information relating to drug therapy and drug reactions, the reader is urged to check the package insert for each drug for any changes in indications and dosage and for added warnings and precautions. This is particularly important when the recommended agent is a new and/or infrequently employed drug.
Disclaimer: The statements, opinions and data contained in this publication are solely those of the individual authors and contributors and not of the publishers and the editor(s). The appearance of advertisements or/and product references in the publication is not a warranty, endorsement, or approval of the products or services advertised or of their effectiveness, quality or safety. The publisher and the editor(s) disclaim responsibility for any injury to persons or property resulting from any ideas, methods, instructions or products referred to in the content or advertisements.
You do not currently have access to this content.