Lysosomal storage disease with skeletal dysplasia.
- Specialty
- Pediatrics
- Subspecialty
- Pediatrics / Pediatric metabolism
- Sex & age distribution
- Male: affected; Female: affected, equal; Children: yes, onset 1–3 years
- Gene(s) involved
- GALNS, GLB1
- Alternative names & eponyms
- Mucopolysaccharidosis type IV
Etiology & mechanism
Deficiency of GALNS or beta-galactosidase.
Gene(s) involved (2)
Symptoms & signs (6)
In plain terms, someone with Morquio syndrome may experience the following — click any to explore related syndromes:
Same gene(s)
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