What is Larsen syndrome?
Also known as: LS
Larsen syndrome is a rare genetic disorder that babies can be born with. It primarily affects the structure and development of bones, but it can vary widely in its presentation. Common symptoms of Larsen syndrome include clubfeet, scoliosis, a greater range of joint movement than usual (hypermobility) and other abnormalities.
Reviewed by: Scott J Schoenleber, MD
This page was last updated on: 1/29/2019 3:21:13 PM
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