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Watson syndrome
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From Wikipedia, the free encyclopedia
Watson syndrome is an autosomal dominant condition characterized by Lisch nodules of the ocular iris, axillary/inguinal freckling, pulmonary valvular stenosis, relative macrocephaly, short stature, and neurofibromas.[1] Watson syndrome is allelictoNF1, the same gene associated with neurofibromatosis type 1.[2]
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Retrieved from "https://en.wikipedia.org/w/index.php?title=Watson_syndrome&oldid=1222459163"
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