兒童 Blau 綜合征并 Ollier 病一例_Chinese Journal of Reparative and Reconstructive Surgery

Authors：

王子龍 , 潘黎明 , 黃鑫瑞 , 路來金 , 余欣 , 龔洪洋 ,  孫希光

吉林大學第一醫院手外科（長春 130021）;

Corresponding?author：

孫希光, Email: xiguangsun@126.com

Keywords：

Blau 綜合征; Ollier 病; NOD2 基因; 基因突變; 兒童

DOI：

10.7507/1002-1892.202011001

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Citation： 王子龍, 潘黎明, 黃鑫瑞, 路來金, 余欣, 龔洪洋, 孫希光. 兒童 Blau 綜合征并 Ollier 病一例. Chinese Journal of Reparative and Reconstructive Surgery, 2021, 35(4): 529-532. doi: 10.7507/1002-1892.202011001 Copy

1.	Rosé CD, Pans S, Casteels I, et al. Blau syndrome: cross-sectional data from a multicentre study of clinical, radiological and functional outcomes. Rheumatology (Oxford), 2015, 54(6): 1008-1016.
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

兒童 Blau 綜合征并 Ollier 病一例

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