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
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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.
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Kamio Y, Kanazawa N, Mine Y, et al. Intractable leg ulcers in Blau syndrome. J Dermatol, 2016, 43(9): 1096-1097.
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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.
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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.
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Silve C, Jüppner H. Ollier disease. Orphanet J Rare Dis, 2006, 1: 37. doi: 10.1186/1750-1172-1-37.
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- 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.
