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Watson syndrome
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Watson syndrome : ウィキペディア英語版
Watson syndrome

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.
== See also ==

* Westerhof syndrome
* List of cutaneous conditions

抄文引用元・出典: フリー百科事典『 ウィキペディア(Wikipedia)
ウィキペディアで「Watson syndrome」の詳細全文を読む



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