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Article

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

BMC pediatrics - 6 Jan 2021

Ge Zhuhui, Mao Jianhua, Shen Huijun, Xu Yu, Fu Haidong, Zhang Weiwei, Li Dongyan

Abstract excerpt

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 disorder on neurogenic bladder have not been reported. Therefore, the aim of the present study is to report two...

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Identifiers

PMID: 33407246
DOI: 10.1186/s12887-020-02484-0
PMCID: PMC7786925

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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