Primary exocrine pancreatic insufficiency in children (a clinical case of Shwachman-Diamond syndrome)

The purpose of the article is to increase the vigilance of clinicians in various fields of medicine to Shwachman-Diamond syndrome in children and to raise awareness of its clinical manifestations, diagnosis and treatment using the example of the case study. An empirical, descriptive study of a clini...

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Main Authors: V.S. Berezenko, Yu.I. Proshchenko, Kh.Z. Mykhayluk, M.B. Dyba, O.M. Tkalik, Yu.O. Savenko
Format: Article
Language:English
Published: Zaslavsky O.Yu. 2024-11-01
Series:Zdorovʹe Rebenka
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Online Access:https://childshealth.zaslavsky.com.ua/index.php/journal/article/view/1759
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author V.S. Berezenko
Yu.I. Proshchenko
Kh.Z. Mykhayluk
M.B. Dyba
O.M. Tkalik
Yu.O. Savenko
author_facet V.S. Berezenko
Yu.I. Proshchenko
Kh.Z. Mykhayluk
M.B. Dyba
O.M. Tkalik
Yu.O. Savenko
author_sort V.S. Berezenko
collection DOAJ
description The purpose of the article is to increase the vigilance of clinicians in various fields of medicine to Shwachman-Diamond syndrome in children and to raise awareness of its clinical manifestations, diagnosis and treatment using the example of the case study. An empirical, descriptive study of a clinical case of Shwachman-Diamond syndrome in a child was conducted. In addition, the literature data from PubMed, Medscape, and CDC were analyzed. Shwachman-Diamond syndrome is an autosomal recessive disease characterized by absolute exocrine pancreatic insufficiency and is the second most common form of primary exocrine pancreatic insufficiency. The diagnosis is made in the presence of a characteristic combination of exocrine pancreatic function disorders, hematologic manifestations (neutropenia, thrombocytopenia, anemia), skeletal abnormalities and is confirmed by molecular genetic testing (mutation in the SBDS gene, which is localized on 7q or 11 and inversion of the 9th chromosome pair). Early diagnosis and timely treatment prevent the onset of adverse symptoms and disability. Treatment is complex and syndromic and includes dietary therapy, enzyme replacement therapy, supplementation with fat-soluble vitamins and correction of hematologic disorders.
format Article
id doaj-art-6ed22ab5020949c7ae61e0098790ffcf
institution Kabale University
issn 2224-0551
2307-1168
language English
publishDate 2024-11-01
publisher Zaslavsky O.Yu.
record_format Article
series Zdorovʹe Rebenka
spelling doaj-art-6ed22ab5020949c7ae61e0098790ffcf2025-01-12T11:28:26ZengZaslavsky O.Yu.Zdorovʹe Rebenka2224-05512307-11682024-11-0119746446910.22141/2224-0551.19.7.2024.17591759Primary exocrine pancreatic insufficiency in children (a clinical case of Shwachman-Diamond syndrome)V.S. Berezenko0https://orcid.org/0000-0002-3777-5251Yu.I. Proshchenko1https://orcid.org/0000-0002-3984-3609Kh.Z. Mykhayluk2https://orcid.org/0000-0002-6720-6674M.B. Dyba3https://orcid.org/0000-0002-9463-7867O.M. Tkalik4https://orcid.org/0000-0002-5449-8399Yu.O. Savenko5https://orcid.org/0000-0002-5224-1610Bogomolets National Medical University, Kyiv, UkraineBogomolets National Medical University, Kyiv, UkraineState Institution “Ukrainian Center of Maternity and Childhood of the National Academy of Medical Sciences of Ukraine”, Kyiv, UkraineState Institution “Ukrainian Center of Maternity and Childhood of the National Academy of Medical Sciences of Ukraine”, Kyiv, UkraineState Institution “Ukrainian Center of Maternity and Childhood of the National Academy of Medical Sciences of Ukraine”, Kyiv, UkraineBogomolets National Medical University, Kyiv, UkraineThe purpose of the article is to increase the vigilance of clinicians in various fields of medicine to Shwachman-Diamond syndrome in children and to raise awareness of its clinical manifestations, diagnosis and treatment using the example of the case study. An empirical, descriptive study of a clinical case of Shwachman-Diamond syndrome in a child was conducted. In addition, the literature data from PubMed, Medscape, and CDC were analyzed. Shwachman-Diamond syndrome is an autosomal recessive disease characterized by absolute exocrine pancreatic insufficiency and is the second most common form of primary exocrine pancreatic insufficiency. The diagnosis is made in the presence of a characteristic combination of exocrine pancreatic function disorders, hematologic manifestations (neutropenia, thrombocytopenia, anemia), skeletal abnormalities and is confirmed by molecular genetic testing (mutation in the SBDS gene, which is localized on 7q or 11 and inversion of the 9th chromosome pair). Early diagnosis and timely treatment prevent the onset of adverse symptoms and disability. Treatment is complex and syndromic and includes dietary therapy, enzyme replacement therapy, supplementation with fat-soluble vitamins and correction of hematologic disorders.https://childshealth.zaslavsky.com.ua/index.php/journal/article/view/1759shwachman-diamond syndromeexocrine pancreatic insufficiencyneutropeniaskeletal abnormalities
spellingShingle V.S. Berezenko
Yu.I. Proshchenko
Kh.Z. Mykhayluk
M.B. Dyba
O.M. Tkalik
Yu.O. Savenko
Primary exocrine pancreatic insufficiency in children (a clinical case of Shwachman-Diamond syndrome)
Zdorovʹe Rebenka
shwachman-diamond syndrome
exocrine pancreatic insufficiency
neutropenia
skeletal abnormalities
title Primary exocrine pancreatic insufficiency in children (a clinical case of Shwachman-Diamond syndrome)
title_full Primary exocrine pancreatic insufficiency in children (a clinical case of Shwachman-Diamond syndrome)
title_fullStr Primary exocrine pancreatic insufficiency in children (a clinical case of Shwachman-Diamond syndrome)
title_full_unstemmed Primary exocrine pancreatic insufficiency in children (a clinical case of Shwachman-Diamond syndrome)
title_short Primary exocrine pancreatic insufficiency in children (a clinical case of Shwachman-Diamond syndrome)
title_sort primary exocrine pancreatic insufficiency in children a clinical case of shwachman diamond syndrome
topic shwachman-diamond syndrome
exocrine pancreatic insufficiency
neutropenia
skeletal abnormalities
url https://childshealth.zaslavsky.com.ua/index.php/journal/article/view/1759
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AT khzmykhayluk primaryexocrinepancreaticinsufficiencyinchildrenaclinicalcaseofshwachmandiamondsyndrome
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