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Medical condition 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 allelic to NF1, the same gene associated with neurofibromatosis type 1.[2]
Watson syndrome | |
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This condition is inherited in an autosomal dominant manner. | |
Specialty | Medical genetics |
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