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Quoted phrase not found in phrase index: "Congenital malabsorptive diarrhea 4"
Page 1
Literature review on congenital glucose-galactose malabsorption from 2001 to 2019.
Wang W, Wang L, Ma M. Wang W, et al. J Paediatr Child Health. 2020 Nov;56(11):1779-1784. doi: 10.1111/jpc.14702. Epub 2020 Sep 18. J Paediatr Child Health. 2020. PMID: 32946683 Review.
AIM: Congenital glucose-galactose malabsorption (CGGM) is a rare disease characterised by severe diarrhoea, dehydration and weight loss. ...Out of 55 cases from Saudi Arabia and Turkey, 43 cases (78.2%) were from consanguineous marriage. Forty-nine cases (73. …
AIM: Congenital glucose-galactose malabsorption (CGGM) is a rare disease characterised by severe diarrhoea, dehydration …
Shwachman-Diamond syndrome: Nationwide survey and systematic review in Japan.
Ikuse T, Kudo T, Arai K, Fujii Y, Ida S, Ishii T, Mushiake S, Nagata K, Tamai H, Toki A, Tomomasa T, Ushijima K, Yanagi T, Yonekura T, Taguchi T, Shimizu T. Ikuse T, et al. Pediatr Int. 2018 Aug;60(8):719-726. doi: 10.1111/ped.13601. Epub 2018 Jul 10. Pediatr Int. 2018. PMID: 29804317 Review.
Although 75% of patients received pancreatic enzyme replacement therapy, there was no significant association between treatment and prognosis. Systematic review identified one clinical practice guideline, two case series, eight case reports and 26 reviews. ...According to …
Although 75% of patients received pancreatic enzyme replacement therapy, there was no significant association between treatment and progn …
Congenital Rare Diseases Causing Persistent Diarrhea in the Newborn: A Single Center Experience.
Hoşnut FÖ, Sahin GE, Ozyazıcı A, Olgac A, Aksu AU. Hoşnut FÖ, et al. Z Geburtshilfe Neonatol. 2022 Oct;226(5):311-318. doi: 10.1055/a-1774-5005. Epub 2022 May 16. Z Geburtshilfe Neonatol. 2022. PMID: 35576965
Congenital diarrheal disorders (CDDs) are a heterogeneous group of inherited diseases that typically occur in the first weeks of life or can present later in life after the introduction of different nutrients; they can cause life-threatening severe dehydration and electrol …
Congenital diarrheal disorders (CDDs) are a heterogeneous group of inherited diseases that typically occur in the first weeks of life …
Congenital Glucose-Galactose Malabsorption: A Case Report.
Anderson S, Koniaris S, Xin B, Brooks SS. Anderson S, et al. J Pediatr Health Care. 2017 Jul-Aug;31(4):506-510. doi: 10.1016/j.pedhc.2017.01.005. Epub 2017 Mar 7. J Pediatr Health Care. 2017. PMID: 28283348
Congenital glucose-galactose malabsorption (CGGM) is a rare cause of intractable infantile diarrhea, with only a few hundred cases recognized worldwide. ...The clinical and diagnostic course of an infant with recurrent episodes of watery diarrhea …
Congenital glucose-galactose malabsorption (CGGM) is a rare cause of intractable infantile diarrhea, with only a few hu …
Intractable diarrhea of infancy: 10 years of experience.
Hizarcioglu-Gulsen H, Saltik-Temizel IN, Demir H, Gurakan F, Ozen H, Yuce A. Hizarcioglu-Gulsen H, et al. J Pediatr Gastroenterol Nutr. 2014 Nov;59(5):571-6. doi: 10.1097/MPG.0000000000000485. J Pediatr Gastroenterol Nutr. 2014. PMID: 25000351
OBJECTIVES: Intractable diarrhea of infancy (IDI), a group of prolonged diarrheal disorders, is difficult to diagnose and manage. ...Carbohydrate malabsorption (CM) and food allergies (n = 11, 18% for both) were the most frequent causes. ...
OBJECTIVES: Intractable diarrhea of infancy (IDI), a group of prolonged diarrheal disorders, is difficult to diagnose and manage. ... …
Exome sequencing finds a novel PCSK1 mutation in a child with generalized malabsorptive diarrhea and diabetes insipidus.
Yourshaw M, Solorzano-Vargas RS, Pickett LA, Lindberg I, Wang J, Cortina G, Pawlikowska-Haddal A, Baron H, Venick RS, Nelson SF, Martín MG. Yourshaw M, et al. J Pediatr Gastroenterol Nutr. 2013 Dec;57(6):759-67. doi: 10.1097/MPG.0b013e3182a8ae6c. J Pediatr Gastroenterol Nutr. 2013. PMID: 24280991 Free PMC article.
OBJECTIVES: Congenital diarrhea disorders are a group of genetically diverse and typically autosomal recessive disorders that have yet to be well characterized phenotypically or molecularly. Diagnostic assessments are generally limited to nutritional challenges and …
OBJECTIVES: Congenital diarrhea disorders are a group of genetically diverse and typically autosomal recessive disorders that …
Tufting enteropathy revisited: the utility of MOC31 (EpCAM) immunohistochemistry in diagnosis.
Ranganathan S, Schmitt LA, Sindhi R. Ranganathan S, et al. Am J Surg Pathol. 2014 Feb;38(2):265-72. doi: 10.1097/PAS.0000000000000106. Am J Surg Pathol. 2014. PMID: 24418860
Other cases of infantile, neonatal, and childhood diarrhea were also retrieved to serve as controls for the staining studies (total 37 patients). ...MOC31 is a diagnostic stain for TE and should be included in the panel in any case of prolonged diarrhea in children …
Other cases of infantile, neonatal, and childhood diarrhea were also retrieved to serve as controls for the staining studies (total 3 …
Microvillous inclusion disease: how to improve the prognosis of a severe congenital enterocyte disorder.
Halac U, Lacaille F, Joly F, Hugot JP, Talbotec C, Colomb V, Ruemmele FM, Goulet O. Halac U, et al. J Pediatr Gastroenterol Nutr. 2011 Apr;52(4):460-5. doi: 10.1097/MPG.0b013e3181fb4559. J Pediatr Gastroenterol Nutr. 2011. PMID: 21407114
BACKGROUND AND OBJECTIVE: Microvillous inclusion disease (MVID) is a rare congenital enterocyte disorder causing severe diarrhea and intestinal failure. ...SBTx, despite being complicated, remains the only hope to improve the quality of life and long-term prognos …
BACKGROUND AND OBJECTIVE: Microvillous inclusion disease (MVID) is a rare congenital enterocyte disorder causing severe diarrhea …
From diarrhea to obesity in prohormone convertase 1/3 deficiency: age-dependent clinical, pathologic, and enteroendocrine characteristics.
Bandsma RH, Sokollik C, Chami R, Cutz E, Brubaker PL, Hamilton JK, Perlman K, Zlotkin S, Sigalet DL, Sherman PM, Martin MG, Avitzur Y. Bandsma RH, et al. J Clin Gastroenterol. 2013 Nov-Dec;47(10):834-43. doi: 10.1097/MCG.0b013e3182a89fc8. J Clin Gastroenterol. 2013. PMID: 24135795 Free PMC article.
BACKGROUND: Prohormone convertases play a pivotal role in the activation of biologically inactive hormones. Congenital defects in the EE axis, such as PC1/3 deficiency, have been rarely reported and their pathophysiological mechanisms are largely unknown. ...RESULTS: All ( …
BACKGROUND: Prohormone convertases play a pivotal role in the activation of biologically inactive hormones. Congenital defects in the …
Congenital sucrase-isomaltase deficiency: identification of a common Inuit founder mutation.
Marcadier JL, Boland M, Scott CR, Issa K, Wu Z, McIntyre AD, Hegele RA, Geraghty MT, Lines MA. Marcadier JL, et al. CMAJ. 2015 Feb 3;187(2):102-107. doi: 10.1503/cmaj.140657. Epub 2014 Dec 1. CMAJ. 2015. PMID: 25452324 Free PMC article.
BACKGROUND: Congenital sucrase-isomaltase deficiency is a rare hereditary cause of chronic diarrhea in children. ...We sought to identify a common mutation for congenital sucrase-isomaltase deficiency in the Inuit population. METHODS: We sequenced the sucrase …
BACKGROUND: Congenital sucrase-isomaltase deficiency is a rare hereditary cause of chronic diarrhea in children. ...We sought …
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