http://chineseinput.net/에서 pinyin(병음)방식으로 중국어를 변환할 수 있습니다.
변환된 중국어를 복사하여 사용하시면 됩니다.
심포지움,특별강연 및 일반연제 발표 : 한국인 상염색체 우성 다낭신 환자의 PKD1과 PKD2 유전자 돌연변이 분석
어현선 ( Eo Hyeon Seon ),안규리 ( An Gyu Li ),채희진 ( Chae Hui Jin ),이은주 ( Lee Eun Ju ),황영환 ( Hwang Yeong Hwan ),황대연 ( Hwang Dae Yeon ),이중건 ( Lee Jung Geon ),김연수 ( Kim Yeon Su ),한진석 ( Han Jin Seog ),김성권 ( Kim 대한신장학회 2000 춘계학술대회 초록집 Vol.19 No.2
생선뼈에 의해 형성된 기관 식도루에서 Fibrinogen-thrombin glue 로 치유된 기관 식도루 1예
조주영,이준성,이문성,심찬섭,유인환,어중건,전동하,이창후,강정협 대한소화기내시경학회 1997 Clinical Endoscopy Vol.17 No.1
Tracheoesophageal fistula is a rare disease of abnormal communication between esopha- gus and respiratory system. The common causes are the acquired origins in adult such as trauma, infection of the adjacent organs, malignant tumor, and foreign body. Among the traumatic origins, chemical drug, the procedure of the dilatation on the stenotic area, blunt trauma(fall, collisions), penetrating trauma(bullet, knife), and pressure injury are much more common than others. Recently, trauma and foreign body in the esophagus and bronchus are becoming the main cause of the tracheoesophageal fistula, however the frequency of the development of tracheoesophageal fistula caused by the infectious diseases is getting decreased. Fibrinogen-thrombin glue stimulates the healing process of the wound and the ulcer. We treated a 52-year-old male patient with nan-inalignant tracheoesophageal fistula, who had symtoms of pharyngolaryngeal and chest discomfort concomitant with a paroxysmal cough on swallowing food which were caused by fish bone. The diagnosis of tracheoesophageal fistula was made by the esophagogram, chest CT, and esop aecopy. By using the therapeutic endoscopy with an injection of the fibrinogen-glue, the tracheoesopeal fistula was obliterated completely with dramatic symptomatic improvement. Here we conqluded that this method would be the one of the best methods for the treatment of tracheoesophageal fistula.
한국인 상염색체 우성 다낭신 가계에서의 유전자 아형분석
한진석,이정상,황영환,김연수,이은주,황대연,이중건,김성권,안규리,어현선,채희진,조종태 대한신장학회 2000 Kidney Research and Clinical Practice Vol.19 No.4
Autosomal dominant polycystic kidney disease (ADPKD) is the most common hereditary renal disease in adults, and its major morbidities are renal failure and cerebrovascular accident. The prevalence of this disease in the chronic haemodialysis patient population is known to be approximately 2% in Korea. So far, three genetic loci have been identified as being responsible for ADPKD, and approximately 85% of the cases in Western countries are related to the PKD1 gene. However, little information is available concerning the pattern of linkage analysis or the mutations present in Asian populations. For this study, 35 families with hereditary renal cysts were recruited from our ADPKD clinic from 1993 to the present, and their molecular genetic characteristics were studied. Subjects were chosen according to the criteria of Ravine et al. Linkage analysis was done with microsatellite makers(PKD1:SM7, UT581, AC2.5, KG8, D16S418, PKD2: D4S423, D4S1534, D4S1542, D4S1544, D4S2460). Genomic DNA PCR and PAGE gel run were done, and the allele patterns were compared with sonographic findings. The results of this study showed that the ratio of PKD1 to PKD2 was 23:3, and PKD2 families showed the tendency of milder renal prognosis than PKD1 families. In conclusion, we confirmed the usefulness of linkage analysis for ADPKD in Korean population, and aur data shows a similar percentage of PKD1(88%) and PKD2(12%) in Korean patients as in the Western population.