Keywords

#watson_syndrome

Watson syndrome

Medical condition

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. Watson syndrome is allelic to NF1, the same gene associated with neurofibromatosis type 1.

Mon 6th

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Watson syndrome Alagille syndrome Noonan syndrome Café au lait spot List of syndromes Westerhof syndrome Moebius syndrome Leaky gut syndrome Down syndrome Lisch nodule
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