儿童 Blau 综合征并 Ollier 病一例_Chinese Journal of Reparative and Reconstructive Surgery

Authors：

王子龙 , 潘黎明 , 黄鑫瑞 , 路来金 , 余欣 , 龚洪洋 ,  孙希光

吉林大学第一医院手外科（长春 130021）;

Corresponding author：

孙希光, Email: xiguangsun@126.com

Keywords：

Blau 综合征; Ollier 病; NOD2 基因; 基因突变; 儿童

DOI：

10.7507/1002-1892.202011001

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Citation： 王子龙, 潘黎明, 黄鑫瑞, 路来金, 余欣, 龚洪洋, 孙希光. 儿童 Blau 综合征并 Ollier 病一例. Chinese Journal of Reparative and Reconstructive Surgery, 2021, 35(4): 529-532. doi: 10.7507/1002-1892.202011001 Copy

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2.	Kamio Y, Kanazawa N, Mine Y, et al. Intractable leg ulcers in Blau syndrome. J Dermatol, 2016, 43(9): 1096-1097.
3.	Li C, Zhang J, Li S, et al. Gene mutations and clinical phenotypes in Chinese children with Blau syndrome. Sci China Life Sci, 2017, 60(7): 758-762.
4.	Ghatan A, Scharschmidt T, Conrad E. Extreme enchondromatosis: a report of two cases and review of the literature. J Bone Joint Surg (Am), 2010, 92(13): 2336-2343.
5.	Silve C, Jüppner H. Ollier disease. Orphanet J Rare Dis, 2006, 1: 37. doi: 10.1186/1750-1172-1-37.

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Chinese Journal of Reparative and Reconstructive Surgery

儿童 Blau 综合征并 Ollier 病一例

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