GALACTOSEMIA IN NEWBORN CHILDREN

GALACTOSEMIA IN NEWBORN CHILDREN

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<em>Galactosemia is a hereditary disease, the pathogenetic treatment of which is based on dietotherapy. Early diagnosing and the adequate choice of the diet improve the development forecasts for the ill child. The article describes a classical galactosemia case in a newborn. It is shown that d...

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Main Authors: G.V. Yatsyk, T.E. Borovik, M.D. Mitish, T.V. Bushueva, E.P. Bombardirova
Format: Article
Language:English
Published: "Paediatrician" Publishers LLC 2007-01-01
Series:Voprosy Sovremennoj Pediatrii
Online Access:http://vsp.spr-journal.ru:80/jour/article/view/1234
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spelling doaj-8898c5041fad40f99eaf6f31849abebd2020-11-24T23:20:09Zeng"Paediatrician" Publishers LLC Voprosy Sovremennoj Pediatrii1682-55271682-55352007-01-01631071111234GALACTOSEMIA IN NEWBORN CHILDRENG.V. Yatsyk0T.E. Borovik1M.D. Mitish2T.V. Bushueva3E.P. Bombardirova4Scientific Center of Children's Health, Russian Academy of Medical Sciences, MoscowScientific Center of Children's Health, Russian Academy of Medical Sciences, MoscowScientific Center of Children's Health, Russian Academy of Medical Sciences, MoscowScientific Center of Children's Health, Russian Academy of Medical Sciences, MoscowScientific Center of Children's Health, Russian Academy of Medical Sciences, Moscow<em>Galactosemia is a hereditary disease, the pathogenetic treatment of which is based on dietotherapy. Early diagnosing and the adequate choice of the diet improve the development forecasts for the ill child. The article describes a classical galactosemia case in a newborn. It is shown that despite diagnosing the disease on the second month of life, the adequate selection of etiopathogenetic dietotherapy and etiotropic therapy of the concurrent diseases helped compensate the inborn galactose metabolism defect and optimize the long-term forecast for the child</em>.<br /><strong><em>Key words: inborn metabolism dysfunctions, alactosemia, dietotherapy, newborn children.</em></strong>http://vsp.spr-journal.ru:80/jour/article/view/1234
collection DOAJ
language English
format Article
sources DOAJ
author G.V. Yatsyk
T.E. Borovik
M.D. Mitish
T.V. Bushueva
E.P. Bombardirova
spellingShingle G.V. Yatsyk
T.E. Borovik
M.D. Mitish
T.V. Bushueva
E.P. Bombardirova
GALACTOSEMIA IN NEWBORN CHILDREN
Voprosy Sovremennoj Pediatrii
author_facet G.V. Yatsyk
T.E. Borovik
M.D. Mitish
T.V. Bushueva
E.P. Bombardirova
author_sort G.V. Yatsyk
title GALACTOSEMIA IN NEWBORN CHILDREN
title_short GALACTOSEMIA IN NEWBORN CHILDREN
title_full GALACTOSEMIA IN NEWBORN CHILDREN
title_fullStr GALACTOSEMIA IN NEWBORN CHILDREN
title_full_unstemmed GALACTOSEMIA IN NEWBORN CHILDREN
title_sort galactosemia in newborn children
publisher "Paediatrician" Publishers LLC
series Voprosy Sovremennoj Pediatrii
issn 1682-5527
1682-5535
publishDate 2007-01-01
description <em>Galactosemia is a hereditary disease, the pathogenetic treatment of which is based on dietotherapy. Early diagnosing and the adequate choice of the diet improve the development forecasts for the ill child. The article describes a classical galactosemia case in a newborn. It is shown that despite diagnosing the disease on the second month of life, the adequate selection of etiopathogenetic dietotherapy and etiotropic therapy of the concurrent diseases helped compensate the inborn galactose metabolism defect and optimize the long-term forecast for the child</em>.<br /><strong><em>Key words: inborn metabolism dysfunctions, alactosemia, dietotherapy, newborn children.</em></strong>
url http://vsp.spr-journal.ru:80/jour/article/view/1234
work_keys_str_mv AT gvyatsyk galactosemiainnewbornchildren
AT teborovik galactosemiainnewbornchildren
AT mdmitish galactosemiainnewbornchildren
AT tvbushueva galactosemiainnewbornchildren
AT epbombardirova galactosemiainnewbornchildren
_version_ 1725575695743057920

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