Literature DB >> 6979240

Lack of lactobezoars in infants given predominantly whey protein formulas.

R L Schreiner, M S Brady, J A Ernst, J A Lemons.   

Abstract

Lactobezoars have been reported with increasing frequency in low-birth-weight infants. The etiology of a lactobezoar is not well understood and is probably multifactorial. During a 2 1/2-year period, 29 of 442 infants weighing less than 2,000 g who were fed casein-predominant formulas had lactobezoars. During the subsequent 14-month period, 223 infants weighing less than 2,000 g were fed a whey-predominant formula, and none had lactobazoars. There have been no reports of lactobezoars in infants fed human milk or whey-predominant formulas. It would appear that the presence of casein as the predominant protein is necessary for the development of a lactobezoar.

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Year:  1982        PMID: 6979240     DOI: 10.1001/archpedi.1982.03970410055012

Source DB:  PubMed          Journal:  Am J Dis Child        ISSN: 0002-922X


  6 in total

1.  Intestinal milk-bolus obstruction in premature infants.

Authors:  B Koletzko
Journal:  Eur J Pediatr       Date:  1989-11       Impact factor: 3.183

2.  Lactobezoar in a low-birth-weight neonate.

Authors:  E R Reddy; S Joseph
Journal:  Can Med Assoc J       Date:  1985-08-15       Impact factor: 8.262

3.  Unusually late presentation of lactobezoar leading to necrotising enterocolitis in an extremely low birthweight infant.

Authors:  Amish Jain; Sunit V Godambe; Simon Clarke; Peter C M Chow
Journal:  BMJ Case Rep       Date:  2009-07-26

Review 4.  Gastric lactobezoar - a rare disorder?

Authors:  Peter Heinz-Erian; Ingmar Gassner; Andreas Klein-Franke; Veronika Jud; Rudolf Trawoeger; Christian Niederwanger; Thomas Mueller; Bernhard Meister; Sabine Scholl-Buergi
Journal:  Orphanet J Rare Dis       Date:  2012-01-04       Impact factor: 4.123

5.  Gastrointestinal obstruction caused by solidification and coagulation of enteral nutrition: pathogenetic mechanisms and potential risk factors.

Authors:  Grazia Leonello; Antonio Giacomo Rizzo; Viviane Di Dio; Antonio Soriano; Claudia Previti; Grazia Giulia Pantè; Claudio Mastrojeni; Sebastiano Pantè
Journal:  Int Med Case Rep J       Date:  2018-04-09

6.  Whole-Exome Sequencing Identified Novel CLMP Mutations in a Family With Congenital Short Bowel Syndrome Presenting Differently in Two Probands.

Authors:  Yao-Hung Chuang; Wen-Lang Fan; Yu-De Chu; Kung-Hao Liang; Yuan-Ming Yeh; Chien-Chang Chen; Cheng-Hsun Chiu; Ming-Wei Lai
Journal:  Front Genet       Date:  2020-12-15       Impact factor: 4.599

  6 in total

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