Mucopolysaccharidosis Type 4 (MPS IV, Morquio Syndrome) Latest Advances

Mucopolysaccharidosis or Skeletal Dysplasia?: Important Clinical and Radiologic Clues for Differential Diagnosis of Based on Difficult Cases.

Journal: Journal of clinical research in pediatric endocrinology

Published: December 04, 2025

Quantification of keratan sulfate in biofluids by validated HPCE-LIF: application to Morquio syndrome.

Journal: Bioanalysis

Published: December 02, 2025

Intraoperative Neuromonitoring Assists in Detecting Positioning-Associated Ischemia in Non-Spine Surgery in Morquio Syndrome: A Case Report.

Journal: A&A practice

Published: November 10, 2025

Management of Neuropsychiatric Symptoms Associated With Morquio Syndrome.

Journal: The primary care companion for CNS disorders

Published: October 01, 2025

Craniovertebral Junction Compression in Patients With Morquio Syndrome: Case Series and Literature Review.

Journal: Cureus

Published: September 23, 2025

Long-Term Liver-Targeted AAV8 Gene Therapy for Mucopolysaccharidosis IVA.

Journal: Current issues in molecular biology

Published: September 12, 2025

Early screening for respiratory and cardiac complications in pediatric mucopolysaccharidosis IVA: Insights from a case.

Journal: Intractable & rare diseases research

Published: September 01, 2025

Mucopolysaccharidosis type IVA and severe hidradenitis suppurativa: A case series.

Journal: JAAD case reports

Published: August 08, 2025

Mucopolysaccharidoses: A biochemical study under limited resources.

Journal: Molecular genetics and metabolism reports

Published: July 14, 2025

Clinical and molecular spectrum of mucopolysaccharidosis IVA in Iraqi children: Allele-specific genotype-phenotype trends and novel GALNS variants.

Journal: Molecular genetics and metabolism reports

Published: July 11, 2025

Neuraminidase 1 secondary deficiency contributes to CNS pathology in neurological mucopolysaccharidoses via brain proteins hypersialylation.

Journal: The Journal of clinical investigation

Published: June 20, 2025

Case report: Successful treatment of a patient presenting with a very rare association of acute lymphoblastic leukemia and mucopolysaccharidosis type IVA.

Journal: Frontiers in pediatrics

Published: June 10, 2025

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Mucopolysaccharidosis or Skeletal Dysplasia?: Important Clinical and Radiologic Clues for Differential Diagnosis of Based on Difficult Cases.

Mucopolysaccharidosis or Skeletal Dysplasia?: Important Clinical and Radiologic Clues for Differential Diagnosis of Based on Difficult Cases.

Quantification of keratan sulfate in biofluids by validated HPCE-LIF: application to Morquio syndrome.

Quantification of keratan sulfate in biofluids by validated HPCE-LIF: application to Morquio syndrome.

Intraoperative Neuromonitoring Assists in Detecting Positioning-Associated Ischemia in Non-Spine Surgery in Morquio Syndrome: A Case Report.

Intraoperative Neuromonitoring Assists in Detecting Positioning-Associated Ischemia in Non-Spine Surgery in Morquio Syndrome: A Case Report.

Management of Neuropsychiatric Symptoms Associated With Morquio Syndrome.

Management of Neuropsychiatric Symptoms Associated With Morquio Syndrome.

Craniovertebral Junction Compression in Patients With Morquio Syndrome: Case Series and Literature Review.

Craniovertebral Junction Compression in Patients With Morquio Syndrome: Case Series and Literature Review.

Long-Term Liver-Targeted AAV8 Gene Therapy for Mucopolysaccharidosis IVA.

Long-Term Liver-Targeted AAV8 Gene Therapy for Mucopolysaccharidosis IVA.

Early screening for respiratory and cardiac complications in pediatric mucopolysaccharidosis IVA: Insights from a case.

Early screening for respiratory and cardiac complications in pediatric mucopolysaccharidosis IVA: Insights from a case.

Mucopolysaccharidosis type IVA and severe hidradenitis suppurativa: A case series.

Mucopolysaccharidosis type IVA and severe hidradenitis suppurativa: A case series.

Mucopolysaccharidoses: A biochemical study under limited resources.

Mucopolysaccharidoses: A biochemical study under limited resources.

Clinical and molecular spectrum of mucopolysaccharidosis IVA in Iraqi children: Allele-specific genotype-phenotype trends and novel GALNS variants.

Clinical and molecular spectrum of mucopolysaccharidosis IVA in Iraqi children: Allele-specific genotype-phenotype trends and novel GALNS variants.

Neuraminidase 1 secondary deficiency contributes to CNS pathology in neurological mucopolysaccharidoses via brain proteins hypersialylation.

Neuraminidase 1 secondary deficiency contributes to CNS pathology in neurological mucopolysaccharidoses via brain proteins hypersialylation.

Case report: Successful treatment of a patient presenting with a very rare association of acute lymphoblastic leukemia and mucopolysaccharidosis type IVA.

Case report: Successful treatment of a patient presenting with a very rare association of acute lymphoblastic leukemia and mucopolysaccharidosis type IVA.