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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
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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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
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
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
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
Goldenhar Syndrome
Babies with Goldenhar Syndrome have facial differences including missing or partial ear, cleft lip/palate and small jaw, and a spine curve. Craniofacial surgeons reconstruct face, ear and palate. Orthopedic surgeons straighten the spine.
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Condition
DiGeorge Syndrome
DiGeorge Syndrome, or 22q11.2 deletion syndrome, is when a small part of chromosome 22 is missing. This results in the poor development of several body systems. Symptoms vary but can include cleft palate.
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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.