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Rare Disease Database

Due to lymphatic system malformations and associated obstruction of normal lymph flow into the bloodstream, affected infants may have an abnormal accumulation of lymph fluid in certain tissues lymphedema. Such surgery is typically performed between 12 and 24 months of age to help prevent the risk of associated infertility. Please note that some of these organizations may provide anal european stomach turner concerning certain conditions potentially associated with this disorder. Because Noonan syndrome is extremely variable and therefore may be under- or misdiagnosed, it may be difficult to determine the true frequency of the disorder in the general population.

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There is also an increased incidence of serious cervical spine disorders, including cervical stenosis, Arnold-Chiari malformation, and syringomyelia. Potentially life-threatening complications may result without appropriate treatment. Alone we are rare. The facial features of individuals with Noonan syndrome tend to change in a predictable manner with age.

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