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[Intestinal microbiocenosis in children with intestinal enzymopathy].

Abstract
141 children with different kinds of intestinal enzymopathy were examined; of these, 33 had celiac disease, 39--the syndrome of celiac disease, 12--congenital lactase deficiency and 57--the syndrome of disaccharidase insufficiency. In these patients a significant decrease in the average characteristics of the main protective flora and the growth of hemolytic and lactose-negative enterobacteria were established. In all groups of patients increased amounts of Proteus were detected, which was indicative of profound dysbiosis. The content of bifidobacteria was found to be decreased in 89.5-97% of the patients and the content of lactic acid bacteria, in 15.8-33.3%. The decreased content of Escherichia coli with normal enzymatic activity (less than 10(7) colony-forming units) was noted in one-third of the patients with the syndrome of celiac disease and congenital lactase deficiency, in about a half of the patients with the syndrome of disaccharidase insufficiency and least of all in patients with celiac disease (9.1%). The association of opportunistic microbes was detected in 15.6% of the patients, more often in those with celiac disease, the syndrome of celiac disease and congenital lactase deficiency. The severity of disturbances in intestinal eubiosis was found to depend on the gravity of the patients' state.
AuthorsA T Kamilova, N N Akhmedov, D B Pulatova, B A Nurmatov
JournalZhurnal mikrobiologii, epidemiologii i immunobiologii (Zh Mikrobiol Epidemiol Immunobiol) 2001 May-Jun Issue 3 Pg. 97-9 ISSN: 0372-9311 [Print] Russia (Federation)
Vernacular TitleSostoianie kishechnogo mikrobiotenoza u deteĭ s kishechnymi énzimopatiiami.
PMID11550576 (Publication Type: English Abstract, Journal Article)
Chemical References
  • Disaccharidases
  • Lactase
  • beta-Galactosidase
Topics
  • Celiac Disease (microbiology)
  • Child
  • Disaccharidases (deficiency)
  • Humans
  • Intestines (enzymology, microbiology)
  • Lactase
  • Syndrome
  • beta-Galactosidase (deficiency)

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