This paper summarized the clinical experience of Professor GE Linyi in treating ulcerative colitis （UC） by stages with the method of clearing. Professor GE believes that the core pathogenesis of UC is dampness and heat in the intestines， and by taking the method of clearing as the basis， he proposed four methods for treatment of UC including clearing and transforming， clearing and dispersing，clearing and moisterning， clearing and nourishing. The pathogenesis of UC in its active stage is dampness and heat in the intestines， congestion and stagnation of qi and blood， and accumulation of stasis toxins， for which the treatment method is to clear and transform， accompanied by clearing and dispersing method. In terms of the clearing and transforming method， Bai Tou Weng Decoction （白头翁汤） combined with Haungqin （Radix Scutellariae）， Machixian （Herba Portulacae） and Pugongying （Herba Taraxaci） is taken as the basic prescription to clear and transform dampness and heat， cool blood， resolve toxins and stop dysentery. For the clearing and dispersing method， medicinals to rectify qi such as Chaihu （Radix Bupleuri）， Cuxiangfu （Vingar Rhizoma Cyperi）， Muxiang （Radix Aucklandiae）， Zhiqiao （Fructus Aurantii）， and Binlang （Semen Arecae）， as well as those to regulate blood such as Danggui （Radix Angelicae Sinensis）， Cebaiye （Cacumen Platycladi） and Diyutan （Radix Sanguisorbae Carbonisatus） are recommended. The pathogenesis of the remission stage is healthy qi depletion and lingering pathogen of dampness and heat stasis toxin in the intestines， for which the method of clearing and nourishing， clearing and moistening can be used； the latter is mainly for people with yin fluids injury， and self-made Qingrun Yichang Decoction （清润益肠汤） is recommended， while the former is for those with spleen and stomach weakness， and self-made Qingyang Jianpi Decoction （清养健脾汤） can be used.

OBJECTIVE: To explore the characteristics of mutations of four common pathogenic genes (GJB2, SLC26A4, GJB3 and 12S rRNA) among patients with nonsyndromic hearing loss (NSHL) from eastern Shandong. METHODS: Peripheral blood samples of 420 NSHL patients were collected, and a hereditary-deafness-gene microarray was used to detect GJB2 c.235delC, c.299-300delAT, c.35delG and c.176del16 mutations, GJB3 c.538C>T mutation, SLC26A4 c.2168A>G and c.IVS7-2A>G mutations, and 12S rRNA c.1555A>C and c.1494C>T mutations. For patients carrying single heterozygous mutations, the coding regions of the above genes were analyzed with Sanger sequencing. RESULTS: The results of the microarray assay and Sanger sequencing showed that 84 patients (20.00%) carried GJB2 mutations, with c.235delC (16.43%) and c.299-300delAT (7.86%) being most common. Seventy-five patients (17.86%) carried SLC26A4 mutations, for which c.IVS7-2A>G accounted for 15.71%. In addition, 5.95% of patients carried 12S rRNA mutations. Only one patient was found to carried GJB3 mutation (c.538C>T). CONCLUSION Common pathogenic mutations for NSHL in eastern Shandong included GJB2 c.235delC and SLC26A4 c.IVS7-2A>G. Of note, 5.95% of patients were due to 12S rRNA m.1555A>G mutation, which gave a frequency greater than other regions of China.
China ; Connexin 26 ; Connexins ; DNA Mutational Analysis ; DNA, Mitochondrial ; Deafness ; Genes, rRNA ; Hearing Loss ; Humans ; Mutation ; RNA, Ribosomal ; Sulfate Transporters