Scheie syndrome is an inherited disease of metabolism in which the body cannot properly break down long chains of sugar molecules called glycosaminoglycans (formerly called mucopolysaccharides).

The syndrome belongs to a group of diseases called mucopolysaccharidoses (MPS). Specifically, it is known as MPS I S.

See also:

• MPS I H (Hurler syndrome)
• MPS II, Hunter syndrome
• MPS IV Morquio syndrome
• MPS III (Sanfilippo syndrome)

Persons with Scheie syndrome are missing a substance called lysosomal alpha-L-iduronidase. This substance, called an enzyme, helps break down long chains of sugar molecules called glycosaminoglycans (formerly called mucopolysaccharides). These molecules are found throughout the body, often in mucus and in fluid around the joints.

Without the enzyme, glycosaminoglycans build up and damage organs, including the heart. Symptoms can range from mild to severe.

Scheie syndrome is the mildest form of mucopolysaccharidosis type 1. The syndrome is syndrome is transmitted as an autosomal recessive trait.

Symptoms may not appear until age 4 or 5, and may include:

• Coarsened facial features
• Increased body hair (hirsutism)
• Broad mouth with full lips
• Cloudy cornea and progressive loss of vision, resulting in blindness
• Prognathism
• Stiff joints
• Claw hands and deformed feet

A physical exam may show signs of:

• Aortic regurgitation
• Hearing loss
• Hernias -- inguinal hernia, umbilical hernia
• Liver swelling
• Prognathism

An eye exam will show cloudy corneas and retinal pigmentation.

Urine tests will be done. Persons with Scheie syndrome have increased amounts of dermatan and heparan sulfate in their urine. See: Urine dermatan sulfate

Other tests may include:

• Blood culture
• Culture of skin fibroblasts
• Echocardiogram
• X-ray of the skeleton