Also known as: LS
What is Larsen syndrome?
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.
What causes Larsen syndrome?
A genetic mutation causes Larsen syndrome. This can occur spontaneously or be passed down from parents to children.
What are the symptoms of Larsen syndrome?
Symptoms of Larsen syndrome can vary widely from person to person. They typically all involve joint or skeletal abnormalities. Possible symptoms include:
What are Larsen syndrome care options?
Treatments for Larsen syndrome are focused on managing specific symptoms and helping individuals with the disease live the best life possible. Different forms of therapy can help with managing the condition, and corrective surgery may be a possibility for some complications of Larsen syndrome.
Reviewed by: Scott J Schoenleber, MD
This page was last updated on: December 18, 2020 05:02 PM
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Cleft Lip and/or Palate
A cleft lip and/or palate is characterized by the presence of a gap (split) in the lip and/or palate seen at birth when the tissues of the lip and/or palate don't come together at all, or come together only part of the way.
Clubfoot is a medical condition in which an infant’s foot or feet are turned inward, either to the side or almost facing upward.