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MPSI Disease Treatment Information for Patients and FamiliesMPSI Disease Treatment Information for Health Care Providers
Patients & Care Givers Overview
About MPS I
What is MPS I?
The MPS Family of Diseases
MPS I Disease Spectrum
What Causes MPS I?
Signs & Symptoms
Diagnosis & Testing
Treatment Options
Patient Stories
Living with MPS I
The MPS I Registry
Resources & Support

Carpal Tunnel Syndrome

People with MPS I sometimes experience pain and loss of feeling in the fingertips as a result of carpal tunnel syndrome. The wrist, or carpus, consists of eight small bones known as the carpals, which are joined by bands called ligaments. A nerve called the median nerve passes through the space between the carpal bones and the ligaments in the wrists. Thickening of the ligaments causes pressure on the median nerve, and this can cause irreversible nerve damage. The nerve damage will cause the muscle at the base of the thumb to waste away and will make it hard for the person with MPS I to use his or her thumb for grasping objects.

Although you or your child may not experience pain, carpal tunnel syndrome may be severe. If you or your child have pain in the hands, particularly at night, you may wish to have an electrical test called a nerve conduction or electromyograph study performed. This test will show whether carpal tunnel syndrome is the cause. If you or your child have any weakness at all in the hand or have problems grasping objects, you may want to ask for the test from your neurologist. Be persistent, as many physicians may not believe that carpal tunnel syndrome is present without the classic symptoms. Most individuals affected by MPS I do not have the classic symptoms of carpal tunnel syndrome, even with severe nerve entrapment and damage. A similar type of nerve compression can happen elsewhere in the body and cause localized weakness or pain.

Carpal Tunnel Syndrome

Courtesy of the National MPS Society

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Did you know...
MPS I is part of the mucopolysaccharidoses (MPS) family, a group of inherited diseases, each caused by accumulation of various glycosaminoglycans (GAGs) in the lysosomes. The exact GAGs that accumulate are different in each case. MPS diseases include seven sub-types and although each of the disorders can cause a variety of different symptoms, many of the diseases share similar symptoms, such as corneal clouding, short stature, and joint stiffness.
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Alicia is a 16-year-old with MPS I who was diagnosed 10 years ago. Watch Alicia’s story to find out how she is handling life as a teenager living with MPS I.
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