-
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.
-
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.
-
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.
-
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.
-
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.
-
Condition
Van Der Woude Syndrome
Van der Woude syndrome is a genetic condition that involves cleft lip, cleft palate, missing teeth, and lip pits. Our multidisciplinary teams provide treatment for physical, emotional and social concerns.
-
Service
Motion Analysis Centers
https://shriners-production-cd.azurewebsites.net/en/Pediatric-Care/Motion-AnalysisThe specialists in Shriners Children’s motion analysis centers collect and analyze movement-related data, like gait analysis, to help treat children with neuromuscular, acquired or congenital disorders.
-
Condition
Sinding-Larsen-Johansson Syndrome
Sinding-Larsen-Johansson syndrome, also called jumper’s knee, manifests as pain at the bottom of the kneecap. It is caused by swelling and irritation of the growth plate in the knee.
-
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 ...
-
Condition
Parry-Romberg Syndrome
Parry-Romberg Syndrome is a rare disease involving shrinking of soft tissue beneath the skin, usually on one side of the face. Shriners Children’s cleft and craniofacial specialists can treat this condition with plastic surgery.