Mucopolysaccharidoses in Brazil: what happens from birth to biochemical diagnosis?

Abstract

Mucopolysaccharidoses (MPS) form a group of inherited metabolic disorders characterized by intralysosomal storage of glycosaminoglycans. This study aimed to investigate the path followed by Brazilian patients from birth to diagnosis. An interview was conducted with patient's parents or guardians with subsequent review of patient's medical records. One hundred thirteen patients with MPS were included (MPS I: 18, MPS II: 43, MPS IIIA: 2, MPS IIIB: 3, MPS IIIC: 1, MPS IVA: 15, MPS IVB: 1, MPS VI: 29, MPS VII: 1) from 97 families. Median age at the onset of signs/symptoms was 18 months (MPS I: 18, MPS II: 24, MPS IVA: 8, MPS VI: 8). Skeletal abnormalities (for MPS IVA and MPS VI), joint contractures (for MPS II), and typical facial features (for MPS I) were the most frequently reported first signs/symptoms. Several health professionals were involved in patient's care as of the onset of symptoms until biochemical diagnosis was established. Median age at diagnosis was 76 months (MPS I: 75, MPS II: 95, MPS IVA: 75, MPS VI: 52). Considering the group as a whole, there was a 4.8-year delay between the onset of signs/symptoms and the establishment of the diagnosis. Considering that specific therapies are available for some of these disorders and that early treatment is likely to change more favorably the natural history of the disease, efforts should be made to minimize this delay. We believe that this situation can be improved by measures that both increase awareness of health professionals about MPS and improve access to diagnostic tests.

DOI: 10.1002/ajmg.a.32320
0100200200920102011201220132014201520162017
Citations per Year

465 Citations

Semantic Scholar estimates that this publication has 465 citations based on the available data.

See our FAQ for additional information.

Cite this paper

@article{Vieira2008MucopolysaccharidosesIB, title={Mucopolysaccharidoses in Brazil: what happens from birth to biochemical diagnosis?}, author={Taiane Alves Vieira and Ida Vanessa Doederlein Schwartz and Ver{\^o}nica Munoz and Louise L. C. Pinto and Carlos Eduardo Steiner and M{\'a}rcia Gonçalves Ribeiro and Raquel Tavares Boy and Victor Evangelista de Faria Ferraz and Ana Carolina de Paula and Chong A E Kim and Angelina Xavier Acosta and Roberto Giugliani}, journal={American journal of medical genetics. Part A}, year={2008}, volume={146A 13}, pages={1741-7} }