Introduction
Larsen Syndrome is a congenital, hereditary condition that primarily affects the musculoskeletal system. It presents with various clinical manifestations and levels of severity.1 Children with highly involved Larsen Syndrome may not survive past infancy, particularly if life-threatening symptoms are not well managed with advanced orthopedic care.9 However, the central nervous system develops normally so cognitive function is intact, and many patients’ symptoms may be orthopedically managed.8
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