Skip to main content

Genetic Counselling for Mediterranean Anaemia in Post-war Greece

  • Chapter
  • First Online:
History of Human Genetics

Abstract

During the twentieth century, haemoglobinopathies and Down syndrome were the most frequent hereditary diseases in Greece. Until the 1950s, medical knowledge concerning the mechanism of hereditary transmission was inadequate, thus making the work of physicians very difficult. It was only in the 1960s when the improvement of medical technology and genetics provided physicians with accurate diagnosis of the most widespread anaemia in Greece, Mediterranean Anaemia or beta-Thalassaemia. In Greece, as in the majority of Mediterranean countries, there was a growing concern for this particular disease, because of the high percentage of carriers in the region. As was often expressed at that period of time (1950–1980), Mediterranean anaemia was the prime social and medical problem.

A carrier of Mediterranean anaemia does not have any apparent symptoms, but the defective gene can be easily diagnosed with a simple blood test. Moreover, a defective gene is expressed only when the person inherits it from both parents. Due to the simplicity of the procedure and the safety of the result, many physicians found themselves obliged to recommend preventive measures, such as a simple blood test.

While some considered the counsellor’s involvement in the decision-making of the parents paternalistic, others thought it imperative. Discussion about genetic counselling prevailed during the period under examination and doctors’ opinions varied. Value-neutral information about the risk of the disease and a non-directive approach were most of the time impossible. However, the dominant view among the doctors was that each prospective parent should take their own responsibility towards this problem.

Since the 1960s, there have been numerous epidemiological studies and abundant statistical data dealing with the incidence of the disease. The first Centre for the prevention of Mediterranean Anaemia was established in Athens in 1975. The blood examination which revealed if someone was a carrier was free of charge. The Greek state funded this centre in Athens and smaller units, incorporated in big hospitals, in the rest of the country.

Although some Mediterranean anaemia experts participated in the meetings of the Hellenic Eugenics Society, the prevention of thalassaemia in Greece was not associated with eugenics. Instead, it became part of the preventive policies of the Greek national healthcare system.

This is a preview of subscription content, log in via an institution to check access.

Access this chapter

Chapter
USD 29.95
Price excludes VAT (USA)
  • Available as PDF
  • Read on any device
  • Instant download
  • Own it forever
eBook
USD 219.00
Price excludes VAT (USA)
  • Available as EPUB and PDF
  • Read on any device
  • Instant download
  • Own it forever
Softcover Book
USD 279.99
Price excludes VAT (USA)
  • Compact, lightweight edition
  • Dispatched in 3 to 5 business days
  • Free shipping worldwide - see info
Hardcover Book
USD 279.99
Price excludes VAT (USA)
  • Durable hardcover edition
  • Dispatched in 3 to 5 business days
  • Free shipping worldwide - see info

Tax calculation will be finalised at checkout

Purchases are for personal use only

Institutional subscriptions

Notes

  1. 1.

    Kattamis et al. 1970, 502–505.

  2. 2.

    See Weatherall 2010.

  3. 3.

    Cao 2010, 62.

  4. 4.

    See Farmaki and Galanello 2011, 272–280.

  5. 5.

    WHO Working Group 1982, 655.

  6. 6.

    Ibid. and Koutelekos and Haliasos 2013, 101–112.

  7. 7.

    See Fessas and Stamaloyannopoulos 1964a; Fessas and Loukopoulos 1964b; Loukopoulos 1965.

  8. 8.

    Caminopetros 1938a, 27–43; Caminopetros 1938b, 104–125.

  9. 9.

    Malamos 1962, 5–13; Cowan 2008, 192.

  10. 10.

    Caminopetros 1952, 687–693.

  11. 11.

    Loukopoulos 2011, 572.

  12. 12.

    Canali and Corbellini 2006.

  13. 13.

    Dronamraju 2006, 2–4.

  14. 14.

    Canali and Corbellini 2006, 58.

  15. 15.

    Angastiniotis and Eleftheriou 2011, 314.

  16. 16.

    Cooley and Lee 1925, 29.

  17. 17.

    Caminopetros 1938a, b.

  18. 18.

    Kattamis et al. 1973; Kattamis 2011b, 330.

  19. 19.

    Kattamis et al. 1979; Kattamis et al. 1982.

  20. 20.

    Kattamis 2011a.

  21. 21.

    Thomas et al. 1982.

  22. 22.

    Loukopoulos 2011.

  23. 23.

    Silvestroni and Bianco 1975; Silvestroni and Bianco 1983.

  24. 24.

    Ashiotis et al. 1973; Angastiniotis et al. 1986.

  25. 25.

    WHO Working Group 1982.

  26. 26.

    Choremis et al. 1963; Fraser et al. 1964; Barnicot et al. 1963; Barnicot et al. 1965.

  27. 27.

    Malamos et al. 1962.

  28. 28.

    Ibid. 11.

  29. 29.

    Hellenic Eugenics Society 1976, 136.

  30. 30.

    Angastiniotis and Eleftherieu 2011, 313.

  31. 31.

    Modell 1977, 495.

  32. 32.

    Hellenic Eugenics Society 1976.

  33. 33.

    Weindling 1997.

  34. 34.

    Dardavesis 2008.

  35. 35.

    Loukopoulos 2011, 573.

  36. 36.

    Ibid. 575.

  37. 37.

    Ibid.

  38. 38.

    Ibid.

  39. 39.

    www.paspama.gr.

  40. 40.

    Ibid.

  41. 41.

    Ibid. 573.

  42. 42.

    Angastiniotis et al. 1986; Ashiotis et al. 1973.

  43. 43.

    Cao et al. 1981.

  44. 44.

    Maniatis 2008.

  45. 45.

    Chatzinikolaou 2002; Mantzarides 2009; Vantsos 2009.

  46. 46.

    Service of Crowning or Marriage. The Great Euchologion of the Orthodox Church 2014, 199.

  47. 47.

    Loukopoulos 2011, 575.

  48. 48.

    Angastiniotis et al. 2011, 314.

  49. 49.

    Modell 1980.

  50. 50.

    See Loukopoulos et al. 1983; Loukopoulos et al. 1988.

  51. 51.

    Loukopoulos et al. 1982.

  52. 52.

    Loukopoulos 2011, 575.

  53. 53.

    Loukopoulos 2016: Interview with the author. Athens, Greece.

  54. 54.

    Hellenic Eugenics Society 1978b, 307.

  55. 55.

    Loukopoulos 2011, 574.

  56. 56.

    Hellenic Eugenics Society 1978b, 303.

  57. 57.

    Hellenic Eugenics Society 1978b, 308.

  58. 58.

    Loukopoulos 2011, 574.

  59. 59.

    Hellenic Eugenics Society 1978b, 308.

  60. 60.

    Aleporou-Marinou et al. 1980; Loukopoulos et al. 1982; Weatherall 2010, 59.

  61. 61.

    Ibid.

  62. 62.

    David 1992; United Nations 2002.

  63. 63.

    Barmpouti 2015, 40–41.

  64. 64.

    Hellenic Eugenics Society 1978b, 306.

  65. 65.

    See Aleporou-Marinou et al. 1980; Loukopoulos 2011.

  66. 66.

    Hellenic Eugenics Society 1965; 1977; 1978.

  67. 67.

    Lane 1955, 198.

  68. 68.

    Bashford 2014.

  69. 69.

    Louros 1955 and 1960.

  70. 70.

    Hellenic Eugenics Society 1978a, 7–28.

  71. 71.

    Hellenic Eugenics Society 1976.

  72. 72.

    Hellenic Eugenics Society 1978b.

  73. 73.

    See Bashford and Levine 2010, 3–24.

  74. 74.

    See Turda 2010.

  75. 75.

    Cowan 2009.

  76. 76.

    Canali and Corbellini 2003, 747.

  77. 77.

    Ibid. 3.

  78. 78.

    Greece. Law 300/1968.

  79. 79.

    Hellenic Eugenics Society 1978b, 302.

  80. 80.

    Hellenic Eugenics Society 1976, 124.

  81. 81.

    Loukopoulos 2011, 574.

References

  • Angastiniotis M, S Kyriakidou, MG Hadjiminas (1986): How Thalassaemia was Controlled in Cyprus. World Health Forum 7: 291-297.

    Google Scholar 

  • Angastiniotis M, A Eleftheriou (2011): The Prevention of Thalassemia-A Review of the International Scene, Haema 2 (3): 313-318.

    Google Scholar 

  • Aleporou-Marinou V et al. (1980): Discussion Paper Prenatal Diagnosis of Thalassemia Major in Greece: Evaluation of the First Large Series of Attempts. Annals of the New York Academy of Sciences 344: 181-188.

    Article  CAS  PubMed  Google Scholar 

  • Ashiotis Th et al. (1973): Thalassaemia in Cyprus. British Medical Journal 2: 38-41.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Barmpouti A (2015): Eugenics and Induced Abortions in post-war Greece. Acta Historiae Medicinae, Stomatologiae, Pharmacie, Veterinae 34 (1): 38-50.

    Google Scholar 

  • Barnicot NA et al. (1963): Haemoglobin Types in Greek populations. Annals of Human Genetics 26:229-236

    Article  CAS  PubMed  Google Scholar 

  • Barnicot NA et al. (1965): A Genetical Survey of Sphakia, Crete. Human Biology 37 (3): 274-298.

    CAS  PubMed  Google Scholar 

  • Bashford A, P Levine (2010): The Oxford Handbook of the History of Eugenics. Oxford: Oxford University Press.

    Book  Google Scholar 

  • Bashford A (2014): Global Population. History, Geopolitics and Life on Earth. New York: Columbia University Press.

    Book  Google Scholar 

  • Caminopetros J. (1938a): Recherches sur l’ Anaemia Erythroblastique Infantile, des Peuples de la Mediterranee Orientale. Premier memoire: étude nosologique. Annals of Medicine 43: 27-43.

    Google Scholar 

  • Caminopetros, J. (1938b), Recherches sur l’ Anaemia Erythroblastique Infantile, des Peoples de la Mediterranee Orientale. Étude anthropologique, étiologique et pathogénique. LaTransmission héréditaire de la maladia. Annals of Medicine 44: 104-125.

    Google Scholar 

  • Caminopetros J. (1952): The Sickle-Cell Anomaly as a Sign of Mediterranean Anaemia. The Lancet 259 (6710): 687-693.

    Article  Google Scholar 

  • Canali S, G Corbellini (2003): Lessons from Anti-thalassemia Campaigns in Italy, before Prenatal Diagnosis. Medicina nei Secoli 14 (3): 739-771.

    Google Scholar 

  • Canali S, G Corbellini (2006) Clinical, Epidemiological, and Genetic Investigations on Thalassemia and Malaria in Italy. In: Dronamraju K, P Arese (2006): Malaria: Genetic and Evolutionary Aspects. New York: Springer. 56-80.

    Google Scholar 

  • Cao, A et al. (1981): Prevention of Homozygous Beta-Thalassaemia by Carrier Screening and Prenatal Diagnosis in Sardinia. American Journal of Human Genetics 33: 592-605.

    CAS  PubMed  PubMed Central  Google Scholar 

  • Cao, A, R Galanello (2010) Beta-Thalassemia. Genetics in Medicine 12 (2): 61-76.

    Article  CAS  PubMed  Google Scholar 

  • Centre of Mediterranean Anaemia, Laiko Hospital Athens [http://www.laiko.gr/index.php?option=com_content&view=article&id=81&Itemid=125 accessed 12 January 2016].

  • Chatzinikolaou, N (2002): Free from genome. Orthodox bioethical approaches. Athens: n.p.

    Google Scholar 

  • Choremis C et al. (1963): Three Inherited Red Cell Abnormalities in a District of Greece. Thalassemia, Sickle Cell and Glucose 6 Dehydrogenase Deficiency. Lancet 281 (7287): 907-910.

    Article  Google Scholar 

  • Cooley, TB, P Lee (1925): Series of Cases of Splenomegaly in Children with Anemia and Peculiar Bone Changes. Transactions of the American Pediatric Society 37: 29-30.

    Google Scholar 

  • Cowan, RS (2008): Heredity and Hope: The Case of Genetic Screening. Cambridge, MA: Harvard Univ. Pr.

    Book  Google Scholar 

  • Cowan, RS (2009): Moving Up the Slippery Slope: Mandating Genetic Screening on Cyprus. American Journal of Medical Genetics, Part C (Seminars in Medical Genetics) 151C: 95-103.

    Google Scholar 

  • Dardavesis, Th. (2008) The Historical Course of the Ministry of Health in Greece, 1833-1981. Iatriko Vima 115: 50-61.

    Google Scholar 

  • David, HP (1992): Abortion in Europe, 1920-91: A public health perspective. Studies in family planning 23 (1): 1-22.

    Article  CAS  PubMed  Google Scholar 

  • Dronamraju, K (2006) Introduction. In: Dronamraju K, P Arese (2006): Malaria: Genetic and Evolutionary Aspects. New York: Springer. 2-15.

    Google Scholar 

  • Farmaki, K (2011): Endocrine Complications in Thalassemia. Haema 2 (3): 272-281.

    CAS  Google Scholar 

  • Fessas, P, G Stamatoyannopoulos (1964a): Hereditary Persistence of Fetal Hemoglobin in Greece. A Study and a Comparison. Blood 24: 223-240.

    CAS  PubMed  Google Scholar 

  • Fessas, P, D Loukopoulos (1964b): Alpha-chain of Human Hemoglobin: Occurrence in vivo. Science 143: 590-591.

    Article  CAS  PubMed  Google Scholar 

  • Fraser, GR et al. (1964): Thalassemias, Abnormal Hemoglobins and G-6PDd in the Arta area of Greece. Annals of the New York Academy of Sciences 119: 415-435.

    Article  CAS  PubMed  Google Scholar 

  • Greece Law 1609 (1986): Artificial termination of pregnancy and woman health protection. Official Government Gazette 86: 2303-2305.

    Google Scholar 

  • Hellenic Eugenics Society (1976): Round Table Discussion: Antenatal Diagnosis. Iatriki 30 (2): 123-187.

    Google Scholar 

  • Hellenic Eugenics Society (1965): Public Discussions, vol. 1. Athens: Parisianos.

    Google Scholar 

  • Hellenic Eugenics Society (1977): Public Discussions, vol. 2. Athens: Parisianos.

    Google Scholar 

  • Hellenic Eugenics Society (1978a): Public Discussions, vol. 3. Athens: Parisianos.

    Google Scholar 

  • Hellenic Eugenics Society (1978b): Premarital Medical Examination. Materia Medica Greca 6 (4): 299-315.

    Google Scholar 

  • Kattamis, C et al. (1970): Growth of Children with Thalassaemia: Effect of Different Transfusion Regimens. Archives of Disease in Childhood 45: 502-505.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Kattamis, C et al. (1973): The Clinical and Hematological Findings in Children Inheriting Two Types of Thalassemia: High A2 Type Beta Thalassemia and High F Type of Delta Beta Thalassemia. British Journal of Haematology 25, 3: 375-384.

    Article  CAS  PubMed  Google Scholar 

  • Kattamis, C et al. (1979): The Heterogeneity of Normal HbA2 β-thalassemia in Greece. British Journal Haematology 42 (1): 109-123.

    Article  CAS  Google Scholar 

  • Kattamis, C et al. (1982): The clinical phenotype of β and δβ Thalassemias in Greece. European Journal of Pediatrics 139, 2: 135-138.

    Article  CAS  PubMed  Google Scholar 

  • Kattamis, C. (1980): Screening for Hemoglobinopathies. In: Bickel H, R Guthrie, G Hammerseng (eds): Neonatal Screening for Inborn Errors of Metabolism. Berlin, Heidelberg: Springer. 133-147.

    Google Scholar 

  • Kattamis, C (2011a): Study and Prevention of Mediterranean Anaemia in Greece in Karamperopoulos D. (ed.): History of Greek Paediatrics. Proceedings of the Fourth Meeting in 2009, Hellenic Society of the History of Paediatrics. Athens.

    Google Scholar 

  • Kattamis, C (2011b): Evolution and Effectiveness of the Greek National Treatment Program for Thalassemia. Haema 2 (3): 330-340.

    Google Scholar 

  • Koutelekos, J, N Haliasos (2013): Mediterranean Anaemia. Perioperative Nursing 2 (3): 101-112.

    Google Scholar 

  • Lane, K (1955): Hellenic Eugenics Society. The Eugenics Review 46 (4): 185.

    Google Scholar 

  • Loukopoulos, D (2011): Haemoglobinopathies in Greece: Prevention Program over the past 35 years. The Indian Journal of Medical Research 134 (4): 572-576.

    PubMed  PubMed Central  Google Scholar 

  • Loukopoulos, D, P Fessas (1965): The Distribution of Hemoglobin Types in Thalassemic Erythrocytes. Journal of Clinical Investigation 44: 231-240.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Loukopoulos, D et al. (1982): Prenatal Diagnosis of Beta-thalassemia; the Greek Experience. Birth Defects Original Article Series 18 (7): 293-301.

    CAS  PubMed  Google Scholar 

  • Loukopoulos, D, A Kaltsoya-Tassiopoulou, P Fessas (1983): Prevention of Thalassemia. Schweizerische Medizinische Wochenschrift 113 (40): 1419-1427.

    CAS  PubMed  Google Scholar 

  • Loukopoulos, D, A Kaltsoya-Tasssiopoulou, P Fessas (1988): Thalassemia Control in Greece. Birth Defects Original Article Series 23 (5B): 405-416.

    CAS  PubMed  Google Scholar 

  • Loukopoulos, D (2016): Interview with the Author. 13.01.2016. Athens, Greece.

    Google Scholar 

  • Louros, N (1955): Eugenics. An appeal. Elliniki Iatriki 24 (1): 289-296.

    Google Scholar 

  • Louros, N (1960): Fertility, Sterility and Overpopulation. International Journal of Fertility 5 (2): 171-173.

    Google Scholar 

  • Malamos, B, Ph Fessas, G Stamatoyannopoulos (1962): Types of Thalassaemia-Trait Carriers as Revealed by a Study of their Incidence in Greece. British Journal of Haematology 8: 5-13.

    Article  CAS  PubMed  Google Scholar 

  • Maniatis, G (2008) Opinion of the Hellenic Bioethics Commission on Prenatal and Preimplantation Genetic Diagnosis, paper presented, 27-28 Nov. 2008. In: 12th Forum of National Ethics Councils, Paris.

    Google Scholar 

  • Mantzarides, G (2009): Christian Ethics. Thessaloniki: Pournaras.

    Google Scholar 

  • Modell, B (1977): Total Management of Thalassaemia Major. Archives of Disease in Childhood 52: 489-500.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Modell, B, RHT Ward, DIVI Fairweather (1980): Effect of Introducing Antenatal Diagnosis on Reproductive Behaviour of Families at Risk for Thalassaemia Major. British Medical Journal 280: 1347-1350.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Pan-Hellenic Association of Patients with Mediterranean Anaemia [www.paspama.gr accessed 11 July 2016]

  • Silvestroni, E, I Bianco (1975): Screening of Microcythaemia in Italy; Analysis of Data Collected in the past 30 years. American Journal of Human Genetics 27: 198-212.

    CAS  PubMed  PubMed Central  Google Scholar 

  • Silvestroni, E, I Bianco (1983): A Highly Cost Effective Method of Mass Screening for Thalassaemia, British Medical Journal 286: 1007-1009.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • The Great Euchologion of the Orthodox Church (2014). Athens: Papadimitriou Publ.

    Google Scholar 

  • Thomas ED, JE Buckner, JE Sanders (1982): Marrow Transplantation for Thalassemia. Lancet 2: 227-229.

    Article  CAS  PubMed  Google Scholar 

  • Turda, M (2010): Modernism and Eugenics. London: Palgrave Macmillan.

    Book  Google Scholar 

  • United Nations (2002): Abortion policies. A global review.

    Google Scholar 

  • Vantsos, M (2009): Ethical Consideration of Abortion. Thessaloniki: Sfakianakis Pub.

    Google Scholar 

  • Weatherall, DJ, JB Clegg (2000): The Thalassemias Syndromes 4th ed. Oxford: Blackwell Scientific Publ.

    Google Scholar 

  • Weatherall, DJ (2010): Thalassaemia. A biography. Oxford: Oxford University Press.

    Google Scholar 

  • Weindling, P (1997): Philanthropy and World Health: The Rockefeller Foundation and the League of Nations Health Organization. Minerva 35: 269-281.

    Article  Google Scholar 

  • WHO Working Group (1982): Hereditary Anaemias: Genetic Basis, Clinical Features, and Treatment. Bulletin of the World Health Organization 60 (5): 643-660.

    PubMed Central  Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Alexandra Barmpouti .

Editor information

Editors and Affiliations

Rights and permissions

Reprints and permissions

Copyright information

© 2017 Springer International Publishing AG

About this chapter

Cite this chapter

Barmpouti, A. (2017). Genetic Counselling for Mediterranean Anaemia in Post-war Greece. In: Petermann, H., Harper, P., Doetz, S. (eds) History of Human Genetics. Springer, Cham. https://doi.org/10.1007/978-3-319-51783-4_27

Download citation

Publish with us

Policies and ethics