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[By contrast, the group of syndromes characterized by keratinocytic nevi comprises three phenotypes with a known molecular etiology in the form of CHILD (congenital hemidysplasia with ichthyosiform nevus and limb defects) syndrome, type 2 segmental Cowden disease, and fibroblast growth factor receptor 3 epidermal nevus syndrome (Garc�a-Hafner-Happle syndrome), whereas Proteus syndrome is still of unknown origin.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
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