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Condition
VATER/VACTERL Syndrome
VATER/VACTERL syndrome is a congenital disorder with at least three irregularities occurring together. VACTERL stands for Vertebral, Anal, Cardiac, Tracheal, Esophageal, Renal (kidney) and Limb abnormalities.
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Condition
Nager Syndrome
Nager Syndrome is a rare condition that affects the development of a child’s face, hands, and arms. Children are born with underdeveloped cheek bones, a small lower jaw, and often have a cleft palate.
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Condition
Crouzon Syndrome
Crouzon syndrome is a rare genetic condition that causes certain skull bones to fuse too early and affects the shape of the child's head and face. Shriners Children's craniofacial specialists offer individualized treatment for this condition.
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Condition
Exertional Compartment Syndrome
Exertional compartment syndrome is a muscle and nerve condition resulting in pain in the lower leg. Most often, it occurs in athletes who participate in high impact sports and is relieved with conservative treatment.
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Condition
Prader-Willi Syndrome
Prader-Willi syndrome is a genetic disorder that affects muscle tone, growth, cognitive behavior and a child’s overall development. It is one of many orthopedic syndromes that are treated at Shriners Children's.
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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
Klippel-Feil Syndrome
Klippel-Feil syndrome occurs when bones in the neck abnormally fuse together before birth. Signs include a short neck, a low hairline at the back of the head or limited ability to turn the neck.
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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.