1.
Ceylon Med J
; 2000 Mar; 45(1): 12-6
Article
in English
| IMSEAR
| ID: sea-47325
ABSTRACT
Beta thalassaemia is a Mendelian recessive disorder. The economic and social cost of the disease is high due to patients' life long need for monthly blood transfusions and treatment with desferrioxamine, an iron chelating agent. Wider availability of cheaper drugs is on the horizon. If there is no concomitant reduction in the number of new thalassaemia major births, there will be a cumulative increase in numbers requiring treatment. The frequency and severity, and the economic and social costs of thalassaemia, support the case for the introduction of a carrier screening and counselling program in Sri Lanka. A three-pronged plan emphasising professional, political and public education in outlined.
Subject(s)
Birth Rate , Consanguinity , Developing Countries/economics , Genetic Counseling , Genetic Testing/methods , Health Care Costs , Genetic Carrier Screening/methods , Humans , Incidence , Sri Lanka/epidemiology , beta-Thalassemia/economics
2.
Ceylon Med J
; 1957 Nov; 4(2): 81-98
Article
in English
| IMSEAR
| ID: sea-47646
3.
Ceylon Med J
; 1956 May; 3(2): 133-9
Article
in English
| IMSEAR
| ID: sea-47744