SciELO - Scientific Electronic Library Online

 
vol.87 número4Nutrición intrahospitalaria del prematuro: Recomendaciones de la Rama de Neonatología de la Sociedad Chilena de Pediatría índice de autoresíndice de materiabúsqueda de artículos
Home Pagelista alfabética de revistas  

Servicios Personalizados

Revista

Articulo

Indicadores

Links relacionados

  • En proceso de indezaciónCitado por Google
  • No hay articulos similaresSimilares en SciELO
  • En proceso de indezaciónSimilares en Google

Compartir


Revista chilena de pediatría

versión impresa ISSN 0370-4106

Resumen

SUAREZ-GUERRERO, Jorge Luis; GOMEZ HIGUERA, Pedro José Iván; ARIAS FLOREZ, Juan Sebastian  y  CONTRERAS-GARCIA, Gustavo Adolfo. Mucopolysaccharidosis: clinical features, diagnosis and management. Rev. chil. pediatr. [online]. 2016, vol.87, n.4, pp.295-304. ISSN 0370-4106.  http://dx.doi.org/10.1016/j.rchipe.2015.10.004.

The mucopolysaccharidoses (MPS) are a group of rare (orphan) diseases, characterised by a deficiency of enzymes involved in the metabolism of glycosaminoglycans (GAGs) at lysosomal level. When there is a deficiency of a particular enzyme there is an accumulation of GAGs in the cells resulting in progressive cellular damage, which can affect multiple organ systems and lead to organ failure. Diagnosis is based on knowledge of the clinical manifestations, performing biochemical analyses to identify the type of GAG that is accumulating, and confirm the type of disorder with the corresponding enzymatic determination. Their identification is essential to initiate early treatment, taking into account that multidisciplinary management and enzyme replacement therapy is available for MPS I (Hurler syndrome), MPS II (Hunter syndrome), MPS IV (Morquio syndrome), and MPS VI (Maroteaux-Lamy syndrome. In this review, an analysis is made of each of these syndromes, as well as their diagnosis and treatment.

Palabras clave : Mucopolysaccharidosis; Sanfilippo syndrome; Hurler syndrome; Hurler-Scheie syndrome; Hunter syndrome; Sly syndrome.

        · resumen en Español     · texto en Español     · Español ( pdf )

 

Creative Commons License Todo el contenido de esta revista, excepto dónde está identificado, está bajo una Licencia Creative Commons