West China Journal of Stomatology ›› 2021, Vol. 39 ›› Issue (2): 230-232.doi: 10.7518/hxkq.2021.02.017

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Basal cell nevus syndrome with Duchenne muscular dystrophy: a case report

Tian Ziyi(), Ma Wen, Zhao Zhiyue, Li Ming()   

  1. Dept. of Oral and Maxillofacial Surgery, Hospital of Stomatology, Kunming Medical University, Kunming 650000, China
  • Received:2020-05-12 Revised:2021-02-01 Online:2021-04-01 Published:2021-04-09
  • Contact: Li Ming E-mail:199712251@qq.com;1020513890@qq.com
  • Supported by:
    General Project of Kunming-Medical Joint Project of Yunnan Province(202001AY070001-250);Kunming Medical University School-level Teaching Research and Teaching Reform Project(2020-JY-Y-041)


Basal cell nevus syndrome (BCNS), also known as Gorlin-Goltz syndrome, is a rare autosomal dominant genetic disease. It is thought to be caused by a mutation in the PTCH1 gene, and its incidence is 1/57 000 to 1/256 000. The case of a 7-year-old patient with BCNS and Duchenne muscular dystrophy was reported in this paper.

Key words: basal cell nevus syndrome, Duchenne muscular dystrophy, odontogenic keratocyst

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