Resumen
Objective: Describing genetic disease frequency in a second-level hospital's in-patient paediatric service Methods: The hospital's statistical department's records for 2005 were comprehensively reviewed; the study was carried out in the town of Ubaté during 2006. Results: Complex diseases led to nearly 25 % of all hospitalisations, including multifactor diseases and congenital malformations. However, an aetiological study and/or geneticist consultation or referral took place on a few occasions. Conclusions: Primary care hospitals should become more relevant reference centres for detecting genetic diseases amongst the paediatric population. New mechanisms are needed for implementing this to allow patients access to a geneticist and for an aetiological diagnosis to be made and providing suitable genetic counselling.
Título traducido de la contribución | Genetic diseases in pediatric patients hospitalised in the town of Ubaté, Colombia |
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Idioma original | Español |
Páginas (desde-hasta) | 414-422 |
Número de páginas | 9 |
Publicación | Revista de Salud Publica |
Volumen | 10 |
N.º | 3 |
DOI | |
Estado | Publicada - jul. 2008 |
Palabras clave
- Consultation
- Genetic load
- Hospital-based
- Referral