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Condition
Williams Syndrome
Williams Syndrome is a genetic condition that can result in weak joints or muscles, learning delays and possible heart issues, with a need for ongoing care. Shriners Children’s can develop a plan to treat the related conditions.
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Condition
T.A.R. Syndrome
Shriners Children physicians treat TAR syndrome, a rare disorder present at birth characterized by low levels of platelets in the blood and absence of the bones of the forearms.
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Condition
Stickler Syndrome
Stickler syndrome, a genetic disorder, involves larger eyes, small nose and chin, cleft palate and joint issues. Craniofacial surgeons repair facial structure and palate. Orthopedic surgeons and rheumatologists treat bone and joints.
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Condition
Nail-Patella Syndrome
Nail-patella syndrome is a rare condition causing irregular growth of the nails, knees, elbows, and pelvis. Symptoms vary in severity, even among members of the same family, and treatment includes bracing or surgery.
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Condition
Ehlers-Danlos Syndrome
Ehlers-Danlos syndrome (EDS) affects the connective tissues, causing joints to become lax or unstable and abnormal skin elasticity. There are varying types. Shriners Children’s works to manage symptoms and improve overall quality of life.
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Condition
Periodic Fever Syndrome
Children with periodic fever syndrome typically have recurring fevers combined with a rash, joint pain or swelling, sores in the mouth and abdominal pain. For treatment, rheumatologists may prescribe anti-inflammatory medication.
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Condition
Freeman-Sheldon Syndrome
Freeman-Sheldon syndrome, or "whistling face syndrome", is a rare condition that primarily affects the face, hands, and feet. From craniofacial to orthopedic specialists, Shriners Children's offers care for many symptoms of this condition.
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Condition
Larsen Syndrome
Larsen syndrome is a rare condition that mostly affects the development of bones. Symptoms vary but commonly include multiple joint dislocations, unusual face structure and a variety of cardiovascular abnormalities.
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Patient Story
Father Credits Burn Team With Saving Daughter's Life
https://www.shrinerschildrens.org/en/News-and-Media/Patient-Stories/2020/10/Father-credits-burn-team-with-saving-daughters-lifeWhen she was 3, Lucy came to Shriners Hospitals for Children — Northern California with Stevens-Johnson syndrome and her life on the line. Chief of Burns David Greenhalgh, M.D., and his team saved her life.
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Condition
Apert Syndrome
Apert Syndrome, also known as acrocephalosyndactyly, is a genetic disorder that presents with deformities of the skull, face and limbs. Symptoms include a high forehead, underdeveloped upper jaw and wide-set eyes. Children can also have problems with their vision and teeth. Craniofacial specialists ...
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