Clinical Presentation and Follow Up of Patients with Mucopolysaccharidosis Type IVA (Morquio A Disease): Single Center Experience

Articles > Article · 2018

Authors: Ebru CANDA, Havva YAZICI, Esra Er, Cenk ERASLAN, Sema KALKAN UÇAR, Mahmut ÇOKER

JOURNAL OF PEDIATRIC RESEARCH, Journal Indexed in SCI Expanded, International, 2018, vol 5, pp 28-33

DOI: 10.4274/jpr.52244

Summary

Aim: Mucopolysaccharidosis Type IVA(MPS IVA), Morquio A, is caused by the deficiency in lysosomal enzyme N-acetylgalactosamine-6-sulfate sulfatase. Multisystemic involvements include skeletal systems, pulmonary disease, valvular heart disease, hearing loss, mild hepatomegaly, corneal clouding, coarse facial features.

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