Cargando…
Ophthalmological Findings in Mucopolysaccharidoses
The mucopolysaccharidoses (MPS) are a heterogenous group of lysosomal storage disorders caused by the accumulation of glycosaminoglycans (GAGs). The accrual of these compounds results in phenotypically varied syndromes that produce multi-organ impairment with widespread systemic effects. The low inc...
Autores principales: | Tomatsu, Shizuka, Pitz, Susanne, Hampel, Ulrike |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2019
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6780167/ https://www.ncbi.nlm.nih.gov/pubmed/31540112 http://dx.doi.org/10.3390/jcm8091467 |
Ejemplares similares
-
Epidemiology of Mucopolysaccharidoses Update
por: Celik, Betul, et al.
Publicado: (2021) -
Ophthalmologic manifestations in Taiwanese patients with mucopolysaccharidoses
por: Lin, Hsiang‐Yu, et al.
Publicado: (2019) -
Evading the AAV Immune Response in Mucopolysaccharidoses
por: Piechnik, Matthew, et al.
Publicado: (2020) -
Hearing Loss in Mucopolysaccharidoses: Current Knowledge and Future Directions
por: Wolfberg, Jeremy, et al.
Publicado: (2020) -
Neonatal cellular and gene therapies for mucopolysaccharidoses: the earlier the better?
por: Tomatsu, Shunji, et al.
Publicado: (2015)