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Acute infantile liver failure syndrome type 2 in a 2.5‐year‐old boy: A case report
KEY CLINICAL MESSAGE: Infantile liver failure type 2 is described as repeated attacks of liver dysfunction with remission. This syndrome should be considered in the differential diagnosis of any child with symptoms of recurrent hepatic encephalopathy. ABSTRACT: Infantile liver failure syndrome 2 is...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10485241/ https://www.ncbi.nlm.nih.gov/pubmed/37692149 http://dx.doi.org/10.1002/ccr3.7892 |
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author | Shabani‐Mirzaee, Hosein Sayarifard, Fatemeh Malekiantaghi, Armen Eftekhari, Kambiz |
author_facet | Shabani‐Mirzaee, Hosein Sayarifard, Fatemeh Malekiantaghi, Armen Eftekhari, Kambiz |
author_sort | Shabani‐Mirzaee, Hosein |
collection | PubMed |
description | KEY CLINICAL MESSAGE: Infantile liver failure type 2 is described as repeated attacks of liver dysfunction with remission. This syndrome should be considered in the differential diagnosis of any child with symptoms of recurrent hepatic encephalopathy. ABSTRACT: Infantile liver failure syndrome 2 is described as recurrent attacks of liver dysfunction. ILFS2 should be included in the differential diagnosis of children with frequent and acute liver failure. We present a 2.5‐year‐old boy with clinical manifestation of acute liver failure. In past, he had two similar attacks. |
format | Online Article Text |
id | pubmed-10485241 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-104852412023-09-09 Acute infantile liver failure syndrome type 2 in a 2.5‐year‐old boy: A case report Shabani‐Mirzaee, Hosein Sayarifard, Fatemeh Malekiantaghi, Armen Eftekhari, Kambiz Clin Case Rep Case Report KEY CLINICAL MESSAGE: Infantile liver failure type 2 is described as repeated attacks of liver dysfunction with remission. This syndrome should be considered in the differential diagnosis of any child with symptoms of recurrent hepatic encephalopathy. ABSTRACT: Infantile liver failure syndrome 2 is described as recurrent attacks of liver dysfunction. ILFS2 should be included in the differential diagnosis of children with frequent and acute liver failure. We present a 2.5‐year‐old boy with clinical manifestation of acute liver failure. In past, he had two similar attacks. John Wiley and Sons Inc. 2023-09-07 /pmc/articles/PMC10485241/ /pubmed/37692149 http://dx.doi.org/10.1002/ccr3.7892 Text en © 2023 The Authors. Clinical Case Reports published by John Wiley & Sons Ltd. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made. |
spellingShingle | Case Report Shabani‐Mirzaee, Hosein Sayarifard, Fatemeh Malekiantaghi, Armen Eftekhari, Kambiz Acute infantile liver failure syndrome type 2 in a 2.5‐year‐old boy: A case report |
title | Acute infantile liver failure syndrome type 2 in a 2.5‐year‐old boy: A case report |
title_full | Acute infantile liver failure syndrome type 2 in a 2.5‐year‐old boy: A case report |
title_fullStr | Acute infantile liver failure syndrome type 2 in a 2.5‐year‐old boy: A case report |
title_full_unstemmed | Acute infantile liver failure syndrome type 2 in a 2.5‐year‐old boy: A case report |
title_short | Acute infantile liver failure syndrome type 2 in a 2.5‐year‐old boy: A case report |
title_sort | acute infantile liver failure syndrome type 2 in a 2.5‐year‐old boy: a case report |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10485241/ https://www.ncbi.nlm.nih.gov/pubmed/37692149 http://dx.doi.org/10.1002/ccr3.7892 |
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