Left-sided valvular heart disease and retinopathy in a 38-year-old woman with attenuated mucopolysaccharidosis: a case report

Mucopolysaccharidoses (MPS) are a group of inherited lysosomal storage disorders caused by deficient levels and/or activity of glycosaminoglycan (GAG)-degradative enzymes. MPS are characterized by accumulation of the mucopolysaccharides heparan sulfate, dermatan sulfate, keratan sulfate, or chondroi...

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Detalles Bibliográficos
Autores principales: Asumda, Faizal Z., Kraker, Jessica A., Thomas, Sarah C., Maleszewski, Joseph, Stone, Edwin M., Lanpher, Brendan C., Schimmenti, Lisa A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2023
Materias:
New therapies in inborn errors of metabolism
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10032445/
https://www.ncbi.nlm.nih.gov/pubmed/37181073
http://dx.doi.org/10.1177/26330040221145945

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10032445/
https://www.ncbi.nlm.nih.gov/pubmed/37181073
http://dx.doi.org/10.1177/26330040221145945

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