نتایج جستجو برای: سندرم سوءجذب malabsorption syndrome

تعداد نتایج: 627685  

2006
A. B. AJDUKIEWICZ A. D. BOUCHIER

Acquired idiopathic hypogammaglobulinaemia can be associated with a sprue-like syndrome in about 20% of patients (Gitlin, Gross, and Janeway, 1959). Hermans, Huizenga, Hoffman, Brown, and Markowitz (1966) described the association of hypogammaglobulinaemia with nodular lymphoid hyperplasia of the small intestine, recurrent upper respiratory infections, the malabsorption syndrome with steatorrho...

Journal: :Vojnosanitetski pregled 2011
Dugan D j Popović Milan Spuran Tamara Alempijević Miodrag Krstić Srdjan Djuranović Nada Kovacević Svetozar Damnjanović Marjan Micev

BACKGROUND Congenital intestinal lymphangiectasia is a disease which leads to protein losing enteropathy. Tortuous, dilated lymphatic vessels in the intestinal wall and mesenterium are typical features of the disease. Clinical manifestations include malabsorption, diarrhea, steatorrhea, edema and effusions. Specific diet and medication are required for disease control. CASE REPORT A 19-year o...

Journal: :Indian pediatrics 2016
Ozlem Yuce Ayhan Gazi Kalayci Atakan Comba Esra Eren Gonul Caltepe

OBJECTIVE To investigate the prevalence of lactose and fructose intolerance in children with chronic abdominal pain. METHODS Hydrogen breath tests were done to detect lactose and fructose malabsorption in 86 children with chronic abdominal pain (44 irritable bowel syndrome, 24 functional abdominal pain and 17 functional abdominal pain syndrome as per Rome III criteria) presenting to a Pediatr...

Journal: :The Journal of pediatrics 2012
Yoon Hi Cho Michel Tchan Bithi Roy Robert Halliday Meredith Wilson Shoma Dutt Susan Siew Craig Munns Neville Howard

ypoparathyroidism-retardation-dysmorphism (HRD) syndrome (OMIM 241410), also known as SanjadSakati syndrome, is a rare autosomal recessive disorder characterized by hypoparathyroidism, growth failure, developmental delay, and characteristic facies. We describe the effective short-term use (tapered over 12 days) of recombinant parathyroid hormone (PTH) (teriparatide) in an unusual genetic condit...

2015
Norman Oneil Machado

Disconnected duct syndrome (DDS) is defined by a complete discontinuity of the pancreatic duct, such that the secretions of pancreas distal to the discontinuity fails to drain into the duodenum. It usually follows acute necrostising pancreatitis. This duct disruption occurs predominately in the pancreatic neck region, which represents a watershed area that is vulnerable to perfusion abnormaliti...

Journal: :Harefuah 1970
S Freier A Drukker R Goldstein L Dollberg

The current policy in this department is to utilize small intestinal biopsy early in the course of investigation of children with suspected malabsorption (Townley, 1971). Also, we have not been unduly hesitant to perform intestinal biopsy in research studies, after the procedure and its risks have been explained to parents (Barnes and Townley, 1973). Others have raised doubts about the safety (...

Journal: :Clinical chemistry 1999
M Ledochowski F Uberall T Propst D Fuchs

Plasma Folic Acid Concentrations in Middle-Aged Subjects, Maximilian Ledochowski, Florian Überall, Theresia Propst, and Dietmar Fuchs (Departments of 1 Clinical Nutrition and 2 Gastroenterology, and 3 Institute of Medical Chemistry and Biochemistry, University of Innsbruck, A-6020 Innsbruck, Austria; * address correspondence to this author at: Institute of Medical Chemistry and Biochemistry, Un...

Journal: :British medical journal 1970
P Karhunen G Härtel V Kivikangas M Reinikainen

It is a pleasure to thank Dr. R. Sears and Mr. P. Dean, of the radioisotope department, the London Hospital, for their help, and Professor J. P. Blandy and Professor H. D. Ritchie for much helpful advice. JOHN R. SALAMAN, M.B., B.CHIR., F.R.C.S. Department of Urology, the London Hospital, London E. 1. REFERENCES Antoine, B., Neveu, T., and Ward, P. D. (1969). Transplantation, 8, 98. Atkins, P.,...

2016

Submit Manuscript | http://medcraveonline.com Abbreviations: BAM: Bile Acid Malabsorption; CA: Cholic Acid; CDCA: Chenodeoxycholic Acid; DCA: Deoxycholic Acid; ASBT: Apical Sodium-dependent Bile Acid Transporter; IBS-D: Diarrhea-Predominant Irritable Bowel Syndrome; SeHCAT: Selenium HomotauroCholic Acid Test, FGF: Fibroblast growth factor; GPBAR1: G Protein-coupled Bile Acid Receptor 1; CYP7A1:...

ژورنال: :مجله علوم پزشکی رازی 0
فهیمه احسانی پور f ehsanipour استادیار و فوق تخصص بیماری های عفونی کودکان، بیمارستان حضرت رسول اکرم(ص)، خیابان ستارخان، خیابان نیایش، دانشگاه علوم پزشکی و خدمات بهداش�

مقدمه: cdls(cornelia de lange syndrome)، سندرم نادری است که با آنومالی های مادرزادی متعدد، عقب ماندگی ذهنی، نمای خاص چهره، تاخیر رشد و نمو، آنومالی های اسکلتی، هیرسوتیسم و درگیری چشمی مشخص می گردد. تشخیص بیماری، کلینیکی است. معرفی بیمار: در این مقاله یک شیرخوار مبتلا به این سندرم معرفی می شود. نتیجه گیری: افزایش آگاهی از این سندرم منجر به تشخیص زودرس و کاهش موربیدیتی می گردد.

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