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Features include: Severe short stature, Fibroblast metachromasia, Cloudy or opaque cornea (corneal opacity), and Platyspondyly and 3 more.
Organ System | Phenotype Count | Example Features |
|---|---|---|
Growth and development | 1 | Severe short stature |
Eyes |
Biomarker and diagnostic research for Morquio syndrome C has been reported in the published literature.
No clinical trials have been registered for Morquio syndrome C.
59 publications have been identified in PubMed for Morquio syndrome C. Research spans Case Report / Case Series (32%), Epidemiology / Natural History (20%), and Basic Science / Preclinical (19%).
Research Type | Count | % of Total |
|---|---|---|
Patient case studies | 19 | 32% |
Data assembled from 4 of 12 sources · Last updated Sep 20, 2026, 11:12 AM UTC
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Online Mendelian Inheritance in Man
Genetic and Rare Diseases Info Center
Common questions about Morquio syndrome C
1
Cloudy or opaque cornea (corneal opacity) |
Brain and nerves | 1 | Intellectual disability |
12 |
20% |
Laboratory research | 11 | 19% |
New treatment approaches | 8 | 14% |
Research summaries | 5 | 8% |
Testing and diagnosis research | 2 | 3% |
Clinical study results | 2 | 3% |
Berti M (2026). [PMID: 41783940](https://pubmed.ncbi.nlm.nih.gov/41783940/). *Dis Model Mech*. [Case Report / Case Series]
Šáhó R (2026). [PMID: 41928800](https://pubmed.ncbi.nlm.nih.gov/41928800/). *Res Sq*. [Epidemiology / Natural History]
Wang M (2026). [PMID: 42081553](https://pubmed.ncbi.nlm.nih.gov/42081553/). *JMIR Pediatr Parent*. [Epidemiology / Natural History]
Reiners N (2026). [PMID: 41182212](https://pubmed.ncbi.nlm.nih.gov/41182212/). *J Hand Surg Am*. [Basic Science / Preclinical]
Stepien KM (2026). [PMID: 42251390](https://pubmed.ncbi.nlm.nih.gov/42251390/). *BMC Health Serv Res*. [Epidemiology / Natural History]
Wijnen M (2026). [PMID: 41987916](https://pubmed.ncbi.nlm.nih.gov/41987916/). *JIMD Rep*. [Case Report / Case Series]
Jafarov S (2026). [PMID: 42173797](https://pubmed.ncbi.nlm.nih.gov/42173797/). *J Voice*. [Case Report / Case Series]
Patel S (2026). [PMID: 41066611](https://pubmed.ncbi.nlm.nih.gov/41066611/). *J Pediatr Orthop*. [Case Report / Case Series]
Pérez-Carmona N (2026). [PMID: 42074270](https://pubmed.ncbi.nlm.nih.gov/42074270/). *Int J Mol Sci*. [Gene Therapy / Novel Therapeutics]
Avendano JP (2026). [PMID: 41733192](https://pubmed.ncbi.nlm.nih.gov/41733192/). *J Pediatr Orthop*. [Case Report / Case Series]
AI-curated news mentioning Morquio syndrome C
Updated Jul 26, 2026
A study published in PubMed examines the effects of early versus late enzyme replacement therapy in siblings with Morquio A syndrome. The findings provide insights into the optimal timing for therapeutic intervention in this rare disease.