REFERENCES
1. Gardner EJ, Richards RC. Multiple cutaneous and subcutaneous lesions
occurring simultaneously with hereditary polyposis and osteomatosis. Am
J Hum Genet. 1953;5(2):139–147.
2. de Oliviera Ribas M, Martins WD, de Sousa MH, et al. Oral and
maxillofacial manifestations of familial adenomatous polyposis
(Gardner’s syndrome): a report of two cases. J Contemp Dent Pract.
2009;10(1):82–90.
3. Shrotriya A, Chaurasia A, Sharma P, Kumari N, Safi S, Rastogi S.
Odontomas: An unusual case series associated with infection and
cutaneous fistula formation. Dentistry. 2018;8:9.
4. Jasperson KW, Patel SG, Ahnen DJ. APC-Associated Polyposis
Conditions. 1998 Dec 18 [Updated 2017 Feb 2]. In: Adam MP, Ardinger
HH, Pagon RA, et al., editors. GeneReviews® [Internet]. Seattle
(WA): University of Washington, Seattle; 1993–2021. Available from:
https://www.ncbi.nlm.nih.gov/books/NBK1345/
5. Iwama T, Tamura K, Morita T, et al. A clinical overview of familial
adenomatous polyposis derived from the database of the Polyposis
Registry of Japan. Int J Clin Oncol. 2004;9(4):308–316.