Blau syndrome with NOD2 mutation in a 54-year-old man: A case report

Blau syndrome (BS) is a rare genetic immune disease which commonly presents in childhood. Currently, the miss-rate of BS diagnosis is very high, and an effective clinical management of BS has not been well established. This case report depicts a 54-year-old male Chinese patient presenting with hand...

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Veröffentlicht in:	International journal of rheumatic diseases 2023-10, Vol.26 (10), p.2080-2084
Hauptverfasser:	Wang, Zhiyan, Yang, Mingdong, Zhang, Qunqun, Zhang, Suhua, Sui, Haifang, Liu, Jiane, Yang, Qingrui
Format:	Artikel
Sprache:	eng
Schlagworte:	Arthralgia Case reports Children Diagnosis Genetic analysis Immunological diseases NOD2 protein
Online-Zugang:	Volltext
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