Albuminuria in patient with Morquio Type A Disease. A case report

  • Sebastián P. Jaurretche Centro de Neurociencias Los Manantiales. Grupo Gamma. Rosario
Keywords: Morquio syndrome, albuminuria, lysosomal storage diseases

References

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Hendriksz CJ, Lavery C, Coker M, Ucar SK, Jain M, Bell L, et al. Burden of disease in patients with Morquio A syndrome: results from an international patient-reported outcomes survey. Orphanet J Rare Dis. 2014;9:32.

Leadley RM, Lang S, Misso K3 Bekkering T, Ross J, Akiyama T, et al. A systematic review of the prevalence of Morquio A syndrome: challenges for study reporting in rare diseases. Orphanet J Rare Dis. 2014;9:173.

Lachman RS, Burton BK, Clarke LA, Hoffinger S, Ikegawa S, Jin DK, et al. Mucopolysaccharidosis IVA (Morquio A syndrome) and VI (Maroteaux-Lamy syndrome): under-recognized and challenging to diagnose. Skeletal Radiol. 2014;43(3):359-69.

Hendriksz CJ, Harmatz P, Beck M, Jones S, Wood T, Lachman R, et al. Review of clinical presentation and diagnosis of mucopolysaccharidosis IVA. Mol Genet Metab. 2013;110(1-2):54-64.

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Hendriksz CJ, Berger KI, Giugliani R, Harmatz P, Kampmann C, Mackenzie WG, et al. International guidelines for the management and treatment of Morquio A syndrome. Am J Med Genet A. 2015;167A(1):11-25.

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Published
2016-06-01
How to Cite
1.
Jaurretche SP. Albuminuria in patient with Morquio Type A Disease. A case report. Rev Nefrol Dial Traspl. [Internet]. 2016Jun.1 [cited 2024Nov.26];36(2):103-7. Available from: http://revistarenal.org.ar/index.php/rndt/article/view/65
Section
Case Report