Clinical and genetic characteristics of concomitant Mucopolysaccharidosis type IVA and neurogenic bladder in children: two case reports and literature review

BACKGROUND: Mucopolysaccharidosis IVA (MPS IVA; Morquio A syndrome) is a rare autosomal recessive lysosomal storage disorder. Up to now, reports on the clinical characteristics of MPS IVA mainly focused on patients with progressive bone dysplasia and multiple organ damage, while the effects of this...

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Detalles Bibliográficos
Autores principales: Ge, Zhuhui, Mao, Jianhua, Shen, Huijun, Xu, Yu, Fu, Haidong, Zhang, Weiwei, Li, Dongyan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7786925/
https://www.ncbi.nlm.nih.gov/pubmed/33407246
http://dx.doi.org/10.1186/s12887-020-02484-0

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7786925/
https://www.ncbi.nlm.nih.gov/pubmed/33407246
http://dx.doi.org/10.1186/s12887-020-02484-0

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