MPS III

Unlike other forms of MPS, symptoms appear after the first year of life. A decline in learning ability typically occurs between ages 2 and 6. The child may have normal growth during the first few years, but final height is below average. Delayed development is followed by deteriorating mental status.

Other symptoms include:

• Behavioral problems
• Coarse facial features
• Diarrhea
• Full lips
• Heavy eyebrows that meet in the middle of the face above the nose
• Sleep difficulties
• Stiff joints that may not extend fully
• Walking problems

A physical exam may show signs of liver and spleen swelling. An eye exam will show clear corneas, unlike the cloudy corneas seen in persons with Hurler syndrome (MPS I H). Neurological testing will reveal signs of seizures and mental retardation.

Urine tests will be done. Persons with Sanfilippo syndrome have large amounts of a mucopolysaccharide called heparan sulfate in the urine.

Other tests may include:

• Blood culture
• Echocardiogram
• Slit lamp eye exam
• Skin fibroblast culture
• X-rays of the bones

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Sanfilippo syndrome Overview

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Sanfilippo syndrome Treatment

Review Date: 05/16/2011
Reviewed By: Chad Haldeman-Englert, MD, Wake Forest School of Medicine, Department of Pediatrics, Section on Medical Genetics, Winston-Salem, NC. Review provided by VeriMed Healthcare Network. Also reviewed by David Zieve, MD, MHA, Medical Director, A.D.A.M., Inc.

A.D.A.M., Inc. is accredited by URAC, also known as the American Accreditation HealthCare Commission (www.urac.org)