Hereditary Fructose Intolerance
Hereditary fructose intolerance, the prevalence of which is 1 : 20,000 population, is diagnosed much less frequently than is found in child and adult populations. Presented pathology is caused by a deficiency in ferment aldolase B and block of fructose transformation in the gastrointestinal tract wi...
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2014-04-01
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doaj-976acbacd2ce4d45853adf0715a1d7f42020-11-24T22:40:02ZengPublishing House ZaslavskyZdorovʹe Rebenka2224-05512307-11682014-04-0193.54929610.22141/2224-0551.3.54.2014.7603976039Hereditary Fructose IntoleranceN.V. Nagornaya0Ye.V. Bordyugova1А.P. Dudchak2А.P. Koval3Donetsk National Medical University named after M. Gorky; Educational and Research Institute of Postgraduate Education, DonetskDonetsk National Medical University named after M. Gorky; Educational and Research Institute of Postgraduate Education, DonetskDonetsk National Medical University named after M. Gorky; Educational and Research Institute of Postgraduate Education, DonetskDonetsk National Medical University named after M. Gorky; Educational and Research Institute of Postgraduate Education, DonetskHereditary fructose intolerance, the prevalence of which is 1 : 20,000 population, is diagnosed much less frequently than is found in child and adult populations. Presented pathology is caused by a deficiency in ferment aldolase B and block of fructose transformation in the gastrointestinal tract with the accumulation of unprocessed fructose in the intestine, manifesting by characteristic symptom and numerous biochemical changes in the body. The disease is asymptomatic until a person begins to use fructose, sucrose or sorbitol. This article describes the fructose metabolism, genetic aspects of the discussing disease, the diversity of its clinical manifestations. The authors presented modern diagnostic criteria and international approaches to diet therapy.http://childshealth.zaslavsky.com.ua/article/view/76039fructosehereditary fructose intolerancealdolase B |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
N.V. Nagornaya Ye.V. Bordyugova А.P. Dudchak А.P. Koval |
spellingShingle |
N.V. Nagornaya Ye.V. Bordyugova А.P. Dudchak А.P. Koval Hereditary Fructose Intolerance Zdorovʹe Rebenka fructose hereditary fructose intolerance aldolase B |
author_facet |
N.V. Nagornaya Ye.V. Bordyugova А.P. Dudchak А.P. Koval |
author_sort |
N.V. Nagornaya |
title |
Hereditary Fructose Intolerance |
title_short |
Hereditary Fructose Intolerance |
title_full |
Hereditary Fructose Intolerance |
title_fullStr |
Hereditary Fructose Intolerance |
title_full_unstemmed |
Hereditary Fructose Intolerance |
title_sort |
hereditary fructose intolerance |
publisher |
Publishing House Zaslavsky |
series |
Zdorovʹe Rebenka |
issn |
2224-0551 2307-1168 |
publishDate |
2014-04-01 |
description |
Hereditary fructose intolerance, the prevalence of which is 1 : 20,000 population, is diagnosed much less frequently than is found in child and adult populations. Presented pathology is caused by a deficiency in ferment aldolase B and block of fructose transformation in the gastrointestinal tract with the accumulation of unprocessed fructose in the intestine, manifesting by characteristic symptom and numerous biochemical changes in the body. The disease is asymptomatic until a person begins to use fructose, sucrose or sorbitol. This article describes the fructose metabolism, genetic aspects of the discussing disease, the diversity of its clinical manifestations. The authors presented modern diagnostic criteria and international approaches to diet therapy. |
topic |
fructose hereditary fructose intolerance aldolase B |
url |
http://childshealth.zaslavsky.com.ua/article/view/76039 |
work_keys_str_mv |
AT nvnagornaya hereditaryfructoseintolerance AT yevbordyugova hereditaryfructoseintolerance AT apdudchak hereditaryfructoseintolerance AT apkoval hereditaryfructoseintolerance |
_version_ |
1725706194273697792 |