2017
DOI: 10.1016/j.bjhh.2017.03.003
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Oral lesions associated with Fanconi anemia

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Cited by 2 publications
(3 citation statements)
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“…Some genetic syndromes that cause dysregulation of DNA metabolism of oral epithelium can lead to premalignant and malignant lesions in this region. Dyskeratosis congenita (Zinsser-Engman-Cole syndrome), Bloom syndrome (BS; congenital telangiectatic erythema), Xeroderma pigmentosum and Fanconi anemia show an increased incidence of OPMDs and OSCC [9,44].…”
Section: Other Risk Factorsmentioning
confidence: 99%
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“…Some genetic syndromes that cause dysregulation of DNA metabolism of oral epithelium can lead to premalignant and malignant lesions in this region. Dyskeratosis congenita (Zinsser-Engman-Cole syndrome), Bloom syndrome (BS; congenital telangiectatic erythema), Xeroderma pigmentosum and Fanconi anemia show an increased incidence of OPMDs and OSCC [9,44].…”
Section: Other Risk Factorsmentioning
confidence: 99%
“…Moreover, chronic mucosal inflammation and oral mucosal trauma from teeth and prosthetic devices have received increasing attention in several clinical and scientific studies [5]. Other suggested factors in common between oral cancer and premalignant lesions are alteration of the microbiome, systemic sclerosis, genetic disease with dysregulation of DNA metabolism (Zinsser-Engman-Cole syndrome, Fanconi anemia and Xeroderma pigmantosum), hematinic and micronutrient deficiency [6][7][8][9].…”
Section: Introductionmentioning
confidence: 99%
“…Fanconi anemia patients are at high risk for oral squamous cell carcinoma. 3 Clinical findings in FA are café au lait spots, short stature, hand abnormality, micrognathia, developmental delay, hyperpigmentation of the neck, cardiac malformation, and many others. Fanconi anemia requires a multidisciplinary follow-up so that appropriate clinical management of patients and their families is achieved.…”
Section: Oral Lesions Associated With Anemia Fanconi Anemiamentioning
confidence: 99%