Mucopolysaccharidosis Type 6 (MPS VI, Maroteaux-Lamy Syndrome) Latest Advances
Find the Latest Research About Mucopolysaccharidosis Type 6 (MPS VI, Maroteaux-Lamy Syndrome)
Last Updated: 06/30/2026
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Found 636 publications
RPE Abnormality Is a Potential Primary Cause for Retinal Degeneration in Mucopolysaccharidosis Type VI Patients and a Rat Model.
Journal: Investigative ophthalmology & visual science
Published: May 18, 2026
A Rare Case of Mucopolysaccharidosis Presenting With Dysostosis Multiplex and Preserved Intelligence in a Seven-Year-Old Girl From Northeast India.
Journal: Cureus
Published: May 14, 2026
Mucopolysaccharidosis Type VI Related Retinopathy.
Journal: Ophthalmology. Retina
Published: April 24, 2026
Acute Airway Crisis in Mucopolysaccharidosis VI: Management Challenges.
Journal: Diagnostics (Basel, Switzerland)
Published: February 24, 2026
Choice of treatment strategy for corneal opacities in patients with mucopolysaccharidosis type VI
Journal: Vestnik oftalmologii
Published: December 23, 2025
Two-year follow-up of musculoskeletal outcomes and quality of life in patients with mucopolysaccharidosis type IV and VI.
Journal: Journal of pediatric endocrinology & metabolism : JPEM
Published: November 23, 2025
Mucopolysaccharidosis type VI in the Russian registry: Further insights and considerations.
Journal: World journal of clinical pediatrics
Published: September 15, 2025
Mucopolysaccharidosis VI: Therapeutic strategies and perspectives.
Journal: Molecular genetics and metabolism
Published: August 26, 2025
Anesthetic Management of Cesarean Section in a Patient With Mucopolysaccharidosis VI (MPS VI): A Case Report.
Journal: Journal of perianesthesia nursing : official journal of the American Society of PeriAnesthesia Nurses
Published: August 24, 2025
Clinical and genetic characteristics of mucopolysaccharidosis type VI according to the Russian registry.
Journal: World journal of clinical pediatrics
Published: May 29, 2025
Last Updated: 06/30/2026