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A unique presentation of hyponatremia and seizures in a 2-month-old child with cystic fibrosis: a case report
Cystic fibrosis is an autosomal recessive disorder that causes a broad range of clinical findings and can present unusually as electrolyte disturbance, such as hyponatremia that causes seizures in children. CASE PRESENTATION: We report a case of a 2-month-old infant who presented with an episode of...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Lippincott Williams & Wilkins
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10406084/ https://www.ncbi.nlm.nih.gov/pubmed/37554905 http://dx.doi.org/10.1097/MS9.0000000000001048 |
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author | Allouzi, Sana Rihawi, Baraa Allouzi, Joud Allouzi, Mohammad I. Abdulrahman, Najwa Abdullah, Manar |
author_facet | Allouzi, Sana Rihawi, Baraa Allouzi, Joud Allouzi, Mohammad I. Abdulrahman, Najwa Abdullah, Manar |
author_sort | Allouzi, Sana |
collection | PubMed |
description | Cystic fibrosis is an autosomal recessive disorder that causes a broad range of clinical findings and can present unusually as electrolyte disturbance, such as hyponatremia that causes seizures in children. CASE PRESENTATION: We report a case of a 2-month-old infant who presented with an episode of grand mal seizure induced by hyponatremia and moderate episodes of milky vomiting after breastfeeding. CLINICAL DISCUSSION: Proper investigations showed normal cardiac and renal functions. Ultrasonography showed no pathological changes. Laboratory tests performed showed hyponatremia, mild hypokalemia, and hypochloremia. Urinary electrolyte results were normal. While broadening the scope of differential diagnosis in order to reach a final diagnosis, the sweat chloride level was elevated, which confirmed the diagnosis of cystic fibroses. CONCLUSION: We aim to share our case to keep cystic fibroses in mind as a differential diagnosis when dealing with hyponatremic seizures in children. |
format | Online Article Text |
id | pubmed-10406084 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Lippincott Williams & Wilkins |
record_format | MEDLINE/PubMed |
spelling | pubmed-104060842023-08-08 A unique presentation of hyponatremia and seizures in a 2-month-old child with cystic fibrosis: a case report Allouzi, Sana Rihawi, Baraa Allouzi, Joud Allouzi, Mohammad I. Abdulrahman, Najwa Abdullah, Manar Ann Med Surg (Lond) Case Reports Cystic fibrosis is an autosomal recessive disorder that causes a broad range of clinical findings and can present unusually as electrolyte disturbance, such as hyponatremia that causes seizures in children. CASE PRESENTATION: We report a case of a 2-month-old infant who presented with an episode of grand mal seizure induced by hyponatremia and moderate episodes of milky vomiting after breastfeeding. CLINICAL DISCUSSION: Proper investigations showed normal cardiac and renal functions. Ultrasonography showed no pathological changes. Laboratory tests performed showed hyponatremia, mild hypokalemia, and hypochloremia. Urinary electrolyte results were normal. While broadening the scope of differential diagnosis in order to reach a final diagnosis, the sweat chloride level was elevated, which confirmed the diagnosis of cystic fibroses. CONCLUSION: We aim to share our case to keep cystic fibroses in mind as a differential diagnosis when dealing with hyponatremic seizures in children. Lippincott Williams & Wilkins 2023-07-08 /pmc/articles/PMC10406084/ /pubmed/37554905 http://dx.doi.org/10.1097/MS9.0000000000001048 Text en Copyright © 2023 The Author(s). Published by Wolters Kluwer Health, Inc. https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the Creative Commons Attribution License 4.0 (https://creativecommons.org/licenses/by/4.0/) (CCBY), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) |
spellingShingle | Case Reports Allouzi, Sana Rihawi, Baraa Allouzi, Joud Allouzi, Mohammad I. Abdulrahman, Najwa Abdullah, Manar A unique presentation of hyponatremia and seizures in a 2-month-old child with cystic fibrosis: a case report |
title | A unique presentation of hyponatremia and seizures in a 2-month-old child with cystic fibrosis: a case report |
title_full | A unique presentation of hyponatremia and seizures in a 2-month-old child with cystic fibrosis: a case report |
title_fullStr | A unique presentation of hyponatremia and seizures in a 2-month-old child with cystic fibrosis: a case report |
title_full_unstemmed | A unique presentation of hyponatremia and seizures in a 2-month-old child with cystic fibrosis: a case report |
title_short | A unique presentation of hyponatremia and seizures in a 2-month-old child with cystic fibrosis: a case report |
title_sort | unique presentation of hyponatremia and seizures in a 2-month-old child with cystic fibrosis: a case report |
topic | Case Reports |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10406084/ https://www.ncbi.nlm.nih.gov/pubmed/37554905 http://dx.doi.org/10.1097/MS9.0000000000001048 |
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