How not to Misdiagnose the Mild Forms of Mucopolysaccharidosisand Juvenile Idiopathic Arthritis
This diagnostic algorithm might increase the suspicion of MPS and should be added to routine testing not miss the mild form of MPS inside JIA. Early diagnosis of mild cases allows for the initiation of treatment in patients with MPS at an earlier stage, which can significantly improve their daily functioning and quality of life.
Authors
- Ekaterina Zakharova (ORCID: https://orcid.org/0000-0002-5020-1180)
- В. И. Ларионова (ORCID: https://orcid.org/0000-0002-3128-8102)
- Lubov S. Sorokina (ORCID: https://orcid.org/0000-0002-9710-9277)
- Dmitry O. Ivanov (ORCID: https://orcid.org/0000-0002-0060-4168)
- Natalia V. Buchinskaya (ORCID: https://orcid.org/0000-0002-2335-3023)
- Natalia V. Zhurkova (ORCID: https://orcid.org/0000-0001-6614-6115)
- Mikhail Mikhaylovich Kostik (ORCID: https://orcid.org/0000-0002-1180-8086)
- Nato D. Vashakmadze (ORCID: https://orcid.org/0000-0001-8320-2027)
- Anastasia O. Vechkasova (ORCID: https://orcid.org/0009-0004-8775-9630)
- Liudmila К. Mikhaylova
Institutions
- Pirogov Russian National Research Medical University (RU)
- Institute of Experimental Medicine (RU)
- Research Centre for Medical Genetics (RU)
- Scientific Center of Children's Health (RU)
- Saint Petersburg State Pediatric Medical University (RU)
Publication Details
- Journal
- Current Pediatric Reviews
- Published
- 2025-07-04
- DOI
- https://doi.org/10.2174/0115733963321478250316112649
- Primary Topic
- Lysosomal Storage Disorders Research
- Type
- article
- Field-Weighted Citation Impact
- 0.00