WordNet

of or relating to or inside the intestines; "intestinal disease" (同)enteric, enteral
present at birth but not necessarily hereditary; acquired during fetal development (同)inborn, innate
an abnormal condition in which a normal opening or tube in the body (as the urethra) is closed or absent

PrepTutorEJDIC

腸[内]の
(病気・身体的欠陥など)生まれつきの,先天的な

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1. 腸管閉鎖症 intestinal atresia
2. 消化管閉鎖症および閉塞の出生前診断 prenatal diagnosis of gastrointestinal atresia and obstruction
3. 先天性肺気道奇形の出生前診断およびマネージメント prenatal diagnosis and management of congenital pulmonary airway malformation
4. 先天性肺気道（嚢胞性腺腫様）形成異常 congenital pulmonary airway cystic adenomatoid malformation
5. 先天性巨大結腸症（ヒルシュスプルング病） congenital aganglionic megacolon hirschsprung disease

English Journal

Cystic Fibrosis as a Rare Cause of Apple Peel Syndrome.

Broekaert IJ, van Koningsbruggen-Rietschel S, Rietschel E.Author information Pediatric Pulmonary, Children's University Hospital Cologne, Germany.AbstractApple peel atresia is a special form of intestinal atresia with absence of mesentery. It is most likely due to an intrauterine intestinal vascular accident and has been described with other anomalies. Meconium ileus can compromise blood supply causing intestinal atresia. Therefore, cystic fibrosis needs to be ruled out in apple peel syndrome.
Klinische Padiatrie.Klin Padiatr.2014 Jan 16. [Epub ahead of print]
Apple peel atresia is a special form of intestinal atresia with absence of mesentery. It is most likely due to an intrauterine intestinal vascular accident and has been described with other anomalies. Meconium ileus can compromise blood supply causing intestinal atresia. Therefore, cystic fibrosis n
PMID 24435787

Mutations in Tetratricopeptide Repeat Domain 7A Result in a Severe Form of Very Early Onset Inflammatory Bowel Disease.

Avitzur Y1, Guo C2, Mastropaolo LA2, Bahrami E3, Chen H4, Zhao Z5, Elkadri A6, Dhillon S2, Murchie R2, Fattouh R2, Huynh H7, Walker JL8, Wales PW9, Cutz E10, Kakuta Y11, Dudley J12, Kammermeier J13, Powrie F14, Shah N13, Walz C15, Nathrath M16, Kotlarz D3, Puchaka J3, Krieger J5, Racek T3, Kirchner T15, Walters TD17, Brumell JH6, Griffiths AM17, Rezaei N18, Rashtian P19, Najafi M19, Monajemzadeh M20, Pelsue S8, McGovern DP21, Uhlig HH22, Schadt E23, Klein C24, Snapper SB25, Muise AM26.Author information 1Group for Improvement of Intestinal Function and Treatment (GIFT), Hospital for Sick Children, Toronto, Ontario, Canada; SickKids Inflammatory Bowel Disease Center and Cell Biology Program, Research Institute, Hospital for Sick Children, Toronto, ON, Canada; Division of Gastroenterology, Hepatology, and Nutrition, Department of Pediatrics, University of Toronto, Hospital for Sick Children, Toronto, ON, Canada; interNational Early Onset Pediatrics IBD Cohort Study (www.NEOPICS.org).2SickKids Inflammatory Bowel Disease Center and Cell Biology Program, Research Institute, Hospital for Sick Children, Toronto, ON, Canada; interNational Early Onset Pediatrics IBD Cohort Study (www.NEOPICS.org).3Department of Pediatrics, Dr. von Hauner Children's Hospital, Ludwig-Maximilians-University, Munich, Germany.4Translational Gastroenterology Unit and Paediatric Gastroenterology, University of Oxford, Oxford, UK.5SickKids Inflammatory Bowel Disease Center and Cell Biology Program, Research Institute, Hospital for Sick Children, Toronto, ON, Canada.6SickKids Inflammatory Bowel Disease Center and Cell Biology Program, Research Institute, Hospital for Sick Children, Toronto, ON, Canada; Division of Gastroenterology, Hepatology, and Nutrition, Department of Pediatrics, University of Toronto, Hospital for Sick Children, Toronto, ON, Canada; Institute of Medical Science, University of Toronto, Toronto, ON, Canada; interNational Early Onset Pediatrics IBD Cohort Study (www.NEOPICS.org).7Division of Pediatric Gastroenterology, Stollery Children's Hospital, Edmonton, ON, Canada; interNational Early Onset Pediatrics IBD Cohort Study (www.NEOPICS.org).8Department of Immunology & Molecular Biology, University of Southern Maine, Maine.9Group for Improvement of Intestinal Function and Treatment (GIFT), Hospital for Sick Children, Toronto, Ontario, Canada.10Division of Pathology, The Hospital for Sick Children, Toronto, Canada.11F. Widjaja Foundation Inflammatory Bowel Disease Center and Immunobiology Research Institute at Cedars-Sinai Medical Center, Los Angeles.12Institute for Genomics and Multiscale Biology, Department of Genetics and Genomics Sciences, Mount Sinai, NY.13Gastroenterology Department, Great Ormond Street Hospital, London, UK.14Translational Gastroenterology Unit, Nuffield Department Clinical Medicine-Experimental Medicine Division, University of Oxford, John Radcliffe Hospital, Oxford, UK; interNational Early Onset Pediatrics IBD Cohort Study (www.NEOPICS.org).15Institute for Pathology, Ludwig-Maximilians University, Munich, Germany.16Department of Pediatric Oncology, Kassel and CCG Osteosarcoma, Helmholtz Center Munich, Germany.17SickKids Inflammatory Bowel Disease Center and Cell Biology Program, Research Institute, Hospital for Sick Children, Toronto, ON, Canada; Division of Gastroenterology, Hepatology, and Nutrition, Department of Pediatrics, University of Toronto, Hospital for Sick Children, Toronto, ON, Canada; interNational Early Onset Pediatrics IBD Cohort Study (www.NEOPICS.org).18Research Center for Immunodeficiencies, Children's Medical Center, Tehran University of Medical Sciences, Tehran, Iran; Molecular Immunology Research Center; and Department of Immunology, School of Medicine, Tehran University of Medical Sciences, Tehran, Iran.19Department of Pediatric Gastroenterology, Children's Medical Center, Tehran University of Medical Sciences, Tehran, Iran.20Department of Pathology, Children's Medical Center, Tehran University of Medical Sciences, Tehran, Iran.21F. Widjaja Foundation Inflammatory Bowel Disease Center and Immunobiology Research Institute at Cedars-Sinai Medical Center, Los Angeles; interNational Early Onset Pediatrics IBD Cohort Study (www.NEOPICS.org).22Translational Gastroenterology Unit and Paediatric Gastroenterology, University of Oxford, Oxford, UK; interNational Early Onset Pediatrics IBD Cohort Study (www.NEOPICS.org).23Institute for Genomics and Multiscale Biology, Department of Genetics and Genomics Sciences, Mount Sinai, NY; interNational Early Onset Pediatrics IBD Cohort Study (www.NEOPICS.org).24Department of Pediatrics, Dr. von Hauner Children's Hospital, Ludwig-Maximilians-University, Munich, Germany; interNational Early Onset Pediatrics IBD Cohort Study (www.NEOPICS.org).25Division of Pediatric Gastroenterology, Hepatology, and Nutrition, Department of Medicine, Children's Hospital Boston; Division of Gastroenterology and Hepatology, Brigham & Women's Hospital, Department of Medicine, Harvard Medical School, Boston, MA; interNational Early Onset Pediatrics IBD Cohort Study (www.NEOPICS.org).26SickKids Inflammatory Bowel Disease Center and Cell Biology Program, Research Institute, Hospital for Sick Children, Toronto, ON, Canada; Division of Gastroenterology, Hepatology, and Nutrition, Department of Pediatrics, University of Toronto, Hospital for Sick Children, Toronto, ON, Canada; Institute of Medical Science, University of Toronto, Toronto, ON, Canada; interNational Early Onset Pediatrics IBD Cohort Study (www.NEOPICS.org). Electronic address: aleixo.muise@utoronto.ca.AbstractBACKGROUND & AIMS: Very early onset inflammatory bowel diseases (VEOIBD), including infant disorders, are a diverse group of diseases found in children less than 6 years of age. They have been associated with several gene variants. We aimed to identify genes that cause VEOIBD.
Gastroenterology.Gastroenterology.2014 Jan 10. pii: S0016-5085(14)00028-6. doi: 10.1053/j.gastro.2014.01.015. [Epub ahead of print]
BACKGROUND & AIMS: Very early onset inflammatory bowel diseases (VEOIBD), including infant disorders, are a diverse group of diseases found in children less than 6 years of age. They have been associated with several gene variants. We aimed to identify genes that cause VEOIBD.METHODS: We perform
PMID 24417819

Japanese Journal

体重5kg未満でgastric transpositionを施行したB型食道閉鎖症の1例

橋詰直樹,飯沼泰史,内藤真一,新田幸壽,平山裕
日本小児外科学会雑誌 47(2), 269-273, 2011-04-20
症例は現在2歳の男児.出生後にGross A型食道閉鎖症,十二指腸閉鎖,直腸肛門奇型と診断し,出生当日に胃瘻造設,人工肛門造設,十二指腸閉鎖根治術を施行した.生後2か月ころより上気道炎から重症肺炎となり,呼吸管理を余儀なくされ,早期の食道閉鎖症根治術が必要と判断した.食道閉鎖は上下食道8椎体long gap症例であったことから,日齢82に全胃吊り上げ食道再建法(gastric transposit …
NAID 110008607772

先天性腸閉鎖症における口径差のある腸吻合の工夫

河崎正裕,高尾智也,片山修一
日本小児外科学会雑誌 47(1), 82-84, 2011-02-20
先天性腸閉鎖症における著しい口径差のある腸吻合法について報告する.われわれの方法は以前Patilが報告したend-to-end linear anastomosisの変法で,口側腸管の吻合口の位置を盲端頂点から腸間膜側にずらし,肛門側腸管は腸間膜対側に切開を加えて径を大きくし,斜めに吻合するものである.これにより吻合部に角度がつかず大きな吻合径が得られる.加えて口側腸管を切除しないため出血や手術時 …
NAID 110008506462

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