Mucopolysaccharidoses (MPS) Latest Advances

Find the Latest Research About Mucopolysaccharidoses (MPS)

Last Updated: 09/19/2026

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Found 3820 publications

Mucopolysaccharidosis type I with retinal degeneration and absence of corneal involvement in the eighth decade of life.

Mucopolysaccharidosis type I with retinal degeneration and absence of corneal involvement in the eighth decade of life.

Journal: Ophthalmic genetics

Published: June 05, 2026

Clinical and Radiological Features Suggestive of Mucopolysaccharidosis in Two Siblings From Sudan: A Case Series.

Clinical and Radiological Features Suggestive of Mucopolysaccharidosis in Two Siblings From Sudan: A Case Series.

Journal: Clinical case reports

Published: May 29, 2026

Advances in Therapies for Mucopolysaccharidoses.

Advances in Therapies for Mucopolysaccharidoses.

Journal: Current issues in molecular biology

Published: May 28, 2026

Homozygous R383H variant in IDUA gene causing pericentric retinitis pigmentosa in attenuated mucopolysaccharidosis type I.

Homozygous R383H variant in IDUA gene causing pericentric retinitis pigmentosa in attenuated mucopolysaccharidosis type I.

Journal: Ophthalmic genetics

Published: May 20, 2026

RPE Abnormality Is a Potential Primary Cause for Retinal Degeneration in Mucopolysaccharidosis Type VI Patients and a Rat Model.

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

Mucopolysaccharidosis type IIIA and IIIC phenotypic progression: A case series.

Mucopolysaccharidosis type IIIA and IIIC phenotypic progression: A case series.

Journal: Molecular genetics and metabolism reports

Published: May 16, 2026

A Rare Case of Mucopolysaccharidosis Presenting With Dysostosis Multiplex and Preserved Intelligence in a Seven-Year-Old Girl From Northeast India.

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

Personalized Drug Repurposing Screen Identifies Patient-Specific Therapeutic Candidates for Mucopolysaccharidosis Type IIIB.

Personalized Drug Repurposing Screen Identifies Patient-Specific Therapeutic Candidates for Mucopolysaccharidosis Type IIIB.

Journal: Journal of personalized medicine

Published: May 12, 2026

Interim analysis of post-marketing surveillance study of intracerebroventricular idursulfase therapy for neuronopathic mucopolysaccharidosis type II: Safety and effectiveness in clinical practice in Japan.

Interim analysis of post-marketing surveillance study of intracerebroventricular idursulfase therapy for neuronopathic mucopolysaccharidosis type II: Safety and effectiveness in clinical practice in Japan.

Journal: Molecular genetics and metabolism

Published: May 08, 2026

Combined Intracerebroventricular Enzyme Replacement and Cord Blood Transplantation in Patients with Mucopolysaccharidosis Type II Diagnosed Through Newborn Screening.

Combined Intracerebroventricular Enzyme Replacement and Cord Blood Transplantation in Patients with Mucopolysaccharidosis Type II Diagnosed Through Newborn Screening.

Journal: International journal of neonatal screening

Published: May 07, 2026

Newborn Screening and Early Cord Blood Transplant for Mucopolysaccharidosis.

Newborn Screening and Early Cord Blood Transplant for Mucopolysaccharidosis.

Journal: JAMA network open

Published: May 04, 2026

Unmasking Mucopolysaccharidosis Type I in a Patient With Wolf-Hirschhorn Syndrome: Diagnostic Overshadowing.

Unmasking Mucopolysaccharidosis Type I in a Patient With Wolf-Hirschhorn Syndrome: Diagnostic Overshadowing.

Journal: JIMD reports

Published: April 29, 2026

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Last Updated: 09/19/2026