Alström syndrome

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Alström syndrome is an inherited disease marked by blindness, deafness, diabetes, and obesity.

Alström syndrome is an autosomal recessive inherited disorder, which means that a person must inherit a copy of the defective gene from both parents in order to be affected. It is extremely rare, but is more common in Holland and Sweden than in the United States.

The mutated gene, ALMS1, has been identified, but it is not yet known how this gene causes the disorder.

Review Date: 12/06/2006
Reviewed By: Ian Marshall, MD, Division of Pediatric Endocrinology, UMDNJ-Robert Wood Johnson Medical School, New Brunswick, NJ. Review provided by VeriMed Healthcare Network.