An estimation of the incidence and demographic picture of the major hemoglobinopathies in Belgium (from a confidential inquiry)
(2008) Hemoglobin : international journal for hemoglobin research — Vol. 32, n° 3, p. 279-285 (2008)
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- An estimation of the incidence and demographic picture of the major hemoglobinopathies in Belgium has been approached through a confidential inquiry sent to 228 pediatric and adult hematological departments. Forty-two percent of responses showed that 417 patients are known in Belgium: 83% with sickle cell disease, 13% with beta-thalassemia (beta-thal) major, 2% with beta-thal intermedia, and 1% with Hb H disease. Twenty-five percent of the sickle cell disease patients and 54% of those suffering from a beta-thal major were older than 20 years. Three hospitals ensure the follow-up of 70% of the patients and are situated in Brussels, Belgium; a follow-up of less than 20 patients was reported at 21 centers. These results confirm that sickle cell disease is the major hemoglobinopathy in Belgium; it concerns mostly pediatricians but adult hematologists are also confronted with these pathologies. Therefore, it is necessary to implement integrated programs of prevention and treatment.
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Gulbis, B., Ferster, A., Vermylen, C., Dresse, M.-F., Vanderfaeillie, A., Delannoy, A., Labarque, V., Philippet, P., Kentos, A., Sztern, B., Deprijck, B., & Vertongen, F. (2008). An estimation of the incidence and demographic picture of the major hemoglobinopathies in Belgium (from a confidential inquiry). Hemoglobin : international journal for hemoglobin research, 32(3), 279-285. https://doi.org/10.1080/03630260802004400 (Original work published 2008)