Organising services for IMD in Thailand: twenty years experience.
- Author:
Pornswan WASANT
1
Author Information
1. Division of Medical Genetics, Department of Pediatrics, Siriraj Hospital, Mahidol University, 2 Prannok road, Siriraj, Bangkoknoi, Bangkok 10700, Thailand. sipws@mahidol.ac.th
- Publication Type:Journal Article
- MeSH:
Child;
Humans;
Metabolism, Inborn Errors;
diagnosis;
epidemiology;
genetics;
Thailand;
Time Factors
- From:Annals of the Academy of Medicine, Singapore
2008;37(12 Suppl):117-113
- CountrySingapore
- Language:English
-
Abstract:
The study of inherited metabolic disorders (IMD) in Thailand is in its infancy when compare with developed countries. Prior to 1987, majority of these disorders were clinically diagnosed since there were only a handful of clinicians and scientists with expertise in inborn errors of metabolism, lack of well-equipped laboratory facilities and government support. In developing countries, inherited metabolic disorders are not considered a priority due to the prevalence of infectious diseases such as HIV infection and congenital infections. A multicentre survey conducted in 1994 and 2001 revealed the existence of numerous cases of IMD from all over the country. Case reports and publications on IMD in Thai (and international) medical journals in past 20 years had undoubtedly raised its awareness among Thai paediatricians and scientists. In 2001, the Genetic Metabolic Centre was first established in Siriraj Hospital Faculty of Medicine, Thailand. Numerous new cases of IMD had been identified since then.
