Type I Neurofibromatosis: Case Report and Review of the Literature Focused on Oral and Cutaneous Les...
Type I Neurofibromatosis: Case Report and Review of the Literature Focused on Oral and Cutaneous Lesions
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Switzerland: MDPI AG
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Language
English
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Switzerland: MDPI AG
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Neurofibromatosis type 1 (NF1) is a common genetic disease whose dermatological lesions are at the forefront of its development. Cutaneous manifestations include café au lait spots, intertriginous freckling, and neurofibromas which appear during childhood and adolescence and are part of the clinical criteria to diagnose NF1. However, it is only rec...
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Type I Neurofibromatosis: Case Report and Review of the Literature Focused on Oral and Cutaneous Lesions
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TN_cdi_doaj_primary_oai_doaj_org_article_401aa2d33ecf40f8b879e19950cdd0eb
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https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_doaj_primary_oai_doaj_org_article_401aa2d33ecf40f8b879e19950cdd0eb
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ISSN
2296-3529
E-ISSN
2296-3529
DOI
10.3390/dermatopathology8010003