Evidence of central nervous system involvement in Watson syndrome.

Abstract excerpt

In 1967, Watson described 3 families with an autosomal dominant condition characterized by pulmonary valvular stenosis, café-au-lait sports, and short stature. Presumed hamartomatous lesions have been observed in neurofibromatosis type I, but they were not reported to date in Watson syndrome. We report another family with Watson syndrome, in which 1 patient manifested increased intensity T2-weighted lesions on...

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