Estimación de las frecuencias de las mucopolisacaridosis y análisis de agrupamiento espacial en los departamentos de cundinamarca y boyacá

Ana Milena Gómez, Reggie García-Robles, Fernando Suárez-Obando

Producción: Contribución a una revistaArtículorevisión exhaustiva

32 Citas (Scopus)

Resumen

Introduction. Mucopolysaccharidoses are a group of infrequent disorders caused by the lysosomal deposit of glycosaminoglycans. Its incidence is quite variable among thecountries where it has been documented. In Brazil, disorder frequencies have been reported, but in Colombia information on them is scarce. Objectives. The frequency and spatial aggregations of the mucopolysaccharidoses were estimated by a retrospective study in two central Colombian provinces. Materials and methods. The records of patients and live newborns between 1998-2007 were reviewed from several reference institutions for genetic diseases. From these records, the frequencies for each mucopolysaccharidosis were estimated. The spatial aggregation of the cases was analyzed using the SaTScan software. Results. The combined frequency for all the mucopolysaccharidoses was 1.98 cases per 100,000 live newborns. MPS IV had the highest frequency with 0.68 cases per 100,000 live newborns and MPS III showed a lower frequency of 0.17/100,000. Three spatial aggregation areas were indicated for MPS I, MPS III and MPS IV. Conclusion. The combined frequency for all the mucopolysaccharidoses has been reported, with type IV the most frequent and the type VII in second place. The data herein constitute a record subset and, in spite of the difficulties inherent to the data retrieval in Colombia, they are a valid estimate of the frequencies of these diseases in central Colombia.

Título traducido de la contribuciónEstimation of the mucopolysaccharidoses frequencies and cluster analysis in the colombian provinces of cundinamarca and boyacá
Idioma originalEspañol
Páginas (desde-hasta)602-609
Número de páginas8
PublicaciónBiomedica
Volumen32
N.º4
DOI
EstadoPublicada - 2012

Palabras clave

  • Cluster analysis
  • Inborn errors
  • Lysosomal storage diseases
  • Metabolism
  • Mucopolysaccharidoses/epidemiology

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