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Results for "scoliosis resources"
Marfan syndrome is a genetic disorder that affects connective tissue, which is the material between cells of the body that
Spinal stenosis is a rare condition characterized by abnormal narrowing (stenosis) of the spaces within the spinal canal,
Ataxia with vitamin E deficiency (AVED) is a rare inherited neurodegenerative disorder characterized by impaired ability
Friedreich's Ataxia is a genetic, progressive, neurologic movement disorder that typically becomes apparent before adolescence.
Ruvalcaba syndrome is a rare inherited disorder characterized by short stature, abnormalities affecting the head and facial
Hypomelanosis of Ito is a rare condition characterized by distinctive skin changes, in which areas of the body lack skin
Congenital fiber type disproportion (CFTD) is a rare genetic muscle disease that is usually apparent at birth (congenital
CDKL5 is a rare X-linked genetic disorder that results in early onset, difficult to control seizures, and severe neurodevelopmental
Post-polio syndrome (PPS) is a syndrome that affects some people who have had polio (poliomyelitis) and occurs many years
Klippel-Feil syndrome (KFS) is a rare skeletal disorder primarily characterized by abnormal union or fusion of two or more