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Published on: May 20, 2019
Joint contractures in the absence of inflammation may indicate mucopolysaccharidosis
Rolando Cimaz1, Giovanni Valentino Coppa, Isabelle Koné-Paut
1Ospedale Meyer-Reumatologia, Firenze, Italy. r.cimaz@meyer.it.
Insights
Rheumatologists can improve early diagnosis of mucopolysaccharidosis (MPS) by using a new algorithm for joint pain. Prompt identification of MPS ensures timely treatment for progressive and debilitating conditions.
Area of Science:
- Rheumatology
- Genetics
- Metabolic Disorders
Background:
- Mucopolysaccharidoses (MPS) are rare genetic lysosomal storage diseases characterized by deficient enzyme activity, leading to glycosaminoglycan accumulation.
- Musculoskeletal manifestations, including joint pain and contractures, are common in MPS, often leading to delayed diagnosis in patients with attenuated forms.
- Current diagnostic rates are low among rheumatologists, highlighting the need for improved recognition and diagnostic tools.
Purpose of the Study:
- To develop and propose a rheumatology-based diagnostic algorithm for identifying mucopolysaccharidosis (MPS) disorders.
- To aid rheumatologists, pediatric rheumatologists, and orthopedists in recognizing and diagnosing MPS based on joint symptoms.
Main Methods:
- The study involved an international working group of rheumatologists and MPS experts.
- Development of a diagnostic algorithm focusing on joint pain and contractures in the absence of inflammation.
- Recommendations for diagnostic testing, including urinary glycosaminoglycan (uGAG) analysis and specific enzyme testing.
Main Results:
- A significant percentage of rheumatologists surveyed (<20%) did not recognize MPS signs or order appropriate diagnostic tests.
- The proposed algorithm aims to increase the recognition of MPS disorders presenting with musculoskeletal symptoms.
- Elevated uGAG levels or abnormal patterns confirm MPS, guiding further specific enzyme testing.
Conclusions:
- Early diagnosis of MPS is crucial for initiating timely and appropriate treatment, preventing long-term disability.
- Rheumatologists play a key role in facilitating early MPS diagnosis through symptom recognition and diagnostic testing.
- The diagnostic algorithm provides a framework for rheumatologists to identify MPS, improving patient outcomes.
Background:
Undiagnosed patients with the attenuated form of mucopolysaccharidosis (MPS) type I often have joint symptoms in childhood that prompt referral to a rheumatologist. A survey conducted by Genzyme Corporation of 60 European and Canadian rheumatologists and pediatric rheumatologists demonstrated that < 20% recognized signs and symptoms of MPS I or could identify appropriate diagnosis tests. These results prompted formation of an international working group of rheumatologists, pediatric rheumatologists, and experts on MPS I to formulate a rheumatology-based diagnostic algorithm. The resulting algorithm applies to all MPS disorders with musculoskeletal manifestations.Bone and joint manifestations are prominent among most patients with MPS disorders. These life-threatening lysosomal storage diseases are caused by deficient activity of specific enzymes involved in the degradation of glycosaminoglycans. Patients with attenuated MPS disease often experience diagnostic delays. Enzyme replacement therapy is now commercially available for MPS I (laronidase), MPS II (idursulfase), and MPS VI (galsulfase).
Presentation Of The Hypothesis:
Evolving joint pain and joint contractures in the absence of inflammation should always raise the suspicion of an MPS disorder. All such patients should undergo urinary glycosaminoglycan (uGAG) analysis (not spot tests for screening) in a reputable laboratory. Elevated uGAG levels and/or an abnormal uGAG pattern confirms an MPS disorder and specific enzyme testing will determine the MPS type. If uGAG analysis is unavailable and the patient exhibits any other common sign or symptom of an MPS disorder, such as corneal clouding, history of hernia surgery, frequent respiratory and/or ear, nose and throat infections; carpal tunnel syndrome, or heart murmur, proceed directly to enzymatic testing. Refer patients with confirmed MPS to a geneticist or metabolic specialist for further evaluation and treatment.
Testing Of The Hypothesis:
We propose that rheumatologists, pediatric rheumatologists, and orthopedists consider our diagnostic algorithm when evaluating patients with joint pain and joint contractures.
Implications Of The Hypothesis:
Children and young adults can suffer for years and sometimes even decades with unrecognized MPS. Rheumatologists may facilitate early diagnosis of MPS based on the presenting signs and symptoms, followed by appropriate testing. Early diagnosis helps ensure prompt and appropriate treatment for these progressive and debilitating diseases.
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