Watson syndrome is a rare genetic condition characterised by brownish patches of skin, short stature, pulmonary stenosis, developmental delays, and learning difficulties. Its inheritance is autosomal dominant, and it may also occur with Lisch nodules of the ocular iris, axillary/inguinal freckling, and neurofibromas.
Watson syndrome is a rare genetic condition characterised by brownish patches of skin, short stature, pulmonary stenosis, developmental delays, and learning difficulties. Its inheritance is autosomal dominant, and it may also occur with Lisch nodules of the ocular iris, axillary/inguinal freckling, and neurofibromas.
Source: Wikipedia "Watson syndrome" · CC BY-SA 4.0
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