• Title/Summary/Keyword: 선천적

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Surgical Correction of a Congenital or Acquired Phimosis in Two Cats (두 마리 고양이에서 선천적 또는 후천적 포피 폐쇄증의 외과적 치료 증례)

  • Yoon, Hun-Young;Jeong, Soon-Wuk
    • Journal of Veterinary Clinics
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    • v.30 no.2
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    • pp.123-126
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    • 2013
  • A 3-month-old male domestic shorthair cat was presented for evaluation of stranguria and hematuria and a 4-year-old male domestic shorthair cat was presented for evaluation of stranguria. For cat 1, a swollen prepuce, erythematous preputial orifice, and urine pooling from the preputial orifice were noted. The preputial orifice was a pinpoint opening and penis was not extruded from the prepuce. For cat 2, a necrotic skin around the preputial orifice, small preputial orifice, and severe urine pooling from the preputial orifice were noted. The round-shaped resection of the tip of the prepuce was performed to increase the diameter of the preputial orifice and remove erythematous fragile skin or a necrotic skin around the preputial orifice and the edematous, redundant preputial mucosa in these 2 cats. The preputial mucosa was then apposed to the ipsilateral incised skin edge. There was no recurrence of clinical signs over 22- and 24-month follow-up period, respectively. The round-shaped resection technique provided adequate enlargement of the preputial orifice to allow extrusion of penis in these 2 cats with a phimosis. This technique could be helpful in cases with skin and mucosa necrosis around the preputial orifice that require round-shaped resection.

Molecular Characterization and Expression Analysis of Nucleoporin 210 (Nup210) in Chicken

  • Ndimukaga, Marc;Bigirwa, Godfrey;Lee, Seokhyun;Lee, Raham;Oh, Jae-Don
    • Korean Journal of Poultry Science
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    • v.46 no.3
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    • pp.185-191
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    • 2019
  • Nucleoporin 210 (Nup210) is associated with several physiological processes including muscle and neural cell differentiation, autoimmune diseases, and peripheral T cell homeostasis. Chicken Nup210 (chNup210) gene was originally identified as one of the differentially expressed genes (DEGs) in the kidney tissues of chicken. To elucidate the role of Nup210 in metabolic disease of chicken, we studied the molecular characteristics of chNup210 and analyzed its gene expression under the stimulation of Toll-like receptor 3 (TLR3) ligands. The Nup210 genomic DNA and amino acid sequences of various species including fowls, fishes, and mammals were retrieved from the Ensemble database and subjected to bioinformatics analyses. The expression of Nup210 from several chicken tissues was probed through qRT-PCR, and chicken fibroblast DF-1 cell line was used to determine the change in expression of chNup210 after stimulation with TLR3 ligand, polyinosinic-polycytidylic acid (poly (I:C)). The chNup210 gene was highly expressed in chicken lung and spleen tissues. Although highly conserved among the species, chNup210 was evolutionary clustered in the same clade as that of duck compared to other mammals. Furthermore, this study revealed that chNup210 is expressed in TLR3 signaling pathway and provides fundamental information on Nup210 expression in chicken. Future studies that offer insight into the involvement of chNup210 in the chicken innate immune response against viral infection are recommended.

An Empirical Analysis of the Characteristics of Entertainers -The 2020 Mr. Trotting Finalists- (예능인에 관한 인상학적 특징 분석 -2020년 미스터트롯 결승진출자를 중심으로-)

  • Youn, Joung-Hye;Kim, Ki-Seung
    • Industry Promotion Research
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    • v.6 no.1
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    • pp.63-77
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    • 2021
  • This study analyzed the impressional characteristics and commonality of the seven people who reached the final final in the 2020 TV Chosun Mister Trot contest, which is the result of the success of the entertainer through the impression. The analysis criteria were set by referring to the classic Ma-uisangbeob and the academic papers on Impressionism, and the faces of seven subjects were collected from the Internet and media. The results of the analysis showed that the following common points were found: First, hair was developed on both sides of the forehead rather than the development of the forehead, which is suitable for arts and physical education rather than studying. Second, most of them had eyebrow bones [the brains of the brain] and cartilage inside their ears was protruding, which is a type of success through effort, deciding on their own life. Third, the mouth was large, the lips were straight, and the neck was thick. This also showed the temperament and talent of artistic ability. Fourth, it developed greatly in the corresponding part by age. In conclusion, while the inherently innate features of facial features cannot prove all that is fatalistic, the characteristic elements of certain talents were clearly manifested. And what they were able to gain and be loved in the entertainment industry was the result of their own efforts beyond it. These results have implications that can be used to determine their talents or career paths in simple aspects.

Laparoscopic Primary Endorectal Pull-through Procedure for Hirschsprung's Disease (선천성 거대결장에서 복강경하 일기적 Boley씨 수술)

  • Kwon, Soo-In
    • Advances in pediatric surgery
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    • v.4 no.2
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    • pp.172-175
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    • 1998
  • With the recent advances in instruments and techniques, laparoscopic procedure have extended to neonates with congenital anomalies. The author reports a 6-day-old boy with Hirschsprung's disease, treated successfully by the laparoscopic endorectall pull-through procedure. The technique and its potential role in the treatment of Hirschsprung's disease are described. One camera port and three working ports were used for access to the peritoneal cavity. The descending and sigmoid colon were mobilized laparoscopically. The submucosal dissection was done transanally. The colon was then pulled down in continuity, divided above the transition zone, and secured to the anal mucosa about 10 mm above the pectinate line. Author concluded that endorectal pull-through can be performed safety with the laparoscope.

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악안면외과 교정술(I)

  • Nam, Il-U
    • The Journal of the Korean dental association
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    • v.21 no.7 s.170
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    • pp.548-549
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    • 1983
  • 악안면외과 교정술은 악골, 안면 혹은 구강에 어떤 기형증에 있을때 이를 외과적 처치에 의하여 개선하거나 치료하는 것을 말한다. 악안면, 구강영역에 발생하는 기형증은 여러가지가 있으나 대체로 비대칭성안모, 악골의 전돌증이나 후퇴증, 개교증, 토순, 구강파열 및 선천성안모발육부전증등 여러 가지가 있다. 본인은 지난 83년 2월부터 5월 초순까지 스위스 쥬리히 치대 악안면외과 교실을 방문하여 이곳 교수들과 접하고 의견을 나누었으며, 강연도 듣고, 하여 주기도 하였다. 또한 이곳 병원에서 외과적안모교정술 등 여러 가지 새로운 시술방법등을 견학하면서 새로운 시술방법을 연구한 바 있다. 지면과 시간이 허락되는 범위안에서 앞으로 수회에 나누어서 악안면외과 교정술에 대하여 구체적으로 소개하고저 한다.

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Surgical Treatment of Congenital Cystic Adenomatoid Malformation; 1 Case Report (선천성 낭종성 기형의 외과적치료;1례 보고)

  • Lee, Jeong-Hui;Im, Jin-Su;Choe, Hyeong-Ho
    • Journal of Chest Surgery
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    • v.26 no.4
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    • pp.320-324
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    • 1993
  • Congenital cystic adenomatoid malformation [CCAM] of the lung is extremely rare. The patient was 10 year old female and had no specipic signs and symptoms except right lower chest pain for 5 days ago before admission.On simple chest X-ray and thoracic CT scan, about 9x8x8cm sized, heterogenous marginal enhanced multiseparated hypodence lesion with air fluid level and gas bubbles in posterior pleural space in right lower chest .The culture result of needle aspiration of cavity was apergillus flavus. Right lower lobectomy was carried out and the result of biopsy was congenital cystic adenomatoid malformation.

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Right Pulmonary Artery Originating Form Ascending Aorta -A Report of Case (상행대동맥에서의 우폐동맥 이상 기시 치험 -1례보고-)

  • 김병철;편승환
    • Journal of Chest Surgery
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    • v.30 no.10
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    • pp.1019-1023
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    • 1997
  • The anomaly which the right pulmonary artery originates from the ascending aorta is a rare and usually fatal form of congenital heart disease. This lesion is often associated with a patent ductus arteriosus. Death frequently occurs in early infancy. Anomalous origin of the right pulmonary artery is much more common than anomalous origin of the left pulmonary artery. The anomalous right pulmonary artery usually arise from the posterior aspect of the ascending aorta close to the aortic valve. We report a 1 month-old infant with right pulmonary artery arising from the ascending aorta, which was corrected successfully by direct anastomosis to the main pul onary artery.

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Tracheal Rupture Following Double-lumen Endotracheal Tube Intubation -One Case Report- (이중관 기관 삽관후 발생된 기관파열 - 1례 보고 -)

  • 박승일;원준호;이종국
    • Journal of Chest Surgery
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    • v.32 no.8
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    • pp.765-767
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    • 1999
  • Tracheobronchial rupture following tracheal intubation is a rare complication. We experienced a case of tracheal rupture following double-lumen endotracheal tube intubation. A 76 year old female was admitted due to coughing and chest discomfort. The operation was performed with the diagnosis of congenital broncho esophageal fistula. During the operation, accidently the main trachea was ruptured longitudinally. There was no history of surgical trauma. The ruptured trachea was repaired with prolene and monofilament absorbable sutures. The cause of tracheal rupture was suspected overinflation of the cuff. The patient was discharged from the hospital without any significant complications.

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Anormalous Origin of Left Coronary Artery from Pulmonary Artery (좌 관상동맥-폐동맥 이상 기시증 수술치험 1례)

  • 조광조;편승환
    • Journal of Chest Surgery
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    • v.30 no.10
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    • pp.1024-1027
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    • 1997
  • Anomalous origin of left coronary artery from pulmonary artery(ALCAPA) is a rare fatal congenital anormaly that needs early surgical intervention. Many reports say that the choice of operative procedure is reimplantation of the left coronary artery into the ascending aorta. We experienced the surgical management of a case of the ALCAPA. The patient was 44 days old and 3.45 kg weighed female baby who had a symptom of congest ve heart failure. She underwent implantation of coronary artery on the aorta with cardiopulmonary bypass and recovered without any complications.

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One Case of Incomplete Double Urethra (선천성 불완전 중복요도 1례)

  • Mo, Seong-Jong;Kim, Young-Soo
    • Journal of Yeungnam Medical Science
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    • v.5 no.2
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    • pp.235-238
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    • 1988
  • Duplication of the urethra within a single penile shaft is a rare anomaly. These can be divided into those that are in the sagittal plane, which is most common, and those that occur side by side. In some cases, the accessory channel is complete, having a separate bladder opening and no communication with the more normal ventral urethra. In other cases, the accessory urethra is incomplete, either ending blindly or communicating with the urethra distal to the bladder neck. We report on a 20-year-old male with incomplete double urethra.

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