Evidence map›Paper›PMID 37554905›Full record

ArticleAnnals of medicine and surgery (2012)2023

A unique presentation of hyponatremia and seizures in a 2-month-old child with cystic fibrosis: a case report.

Sana Allouzi, Baraa Rihawi, Joud Allouzi, Mohammad I Allouzi, Najwa Abdulrahman, Manar Abdullah

Abstract read
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Article in Annals of medicine and surgery (2012), 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

  1. Review
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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Sana AllouziInternal Medicine Department, Endocrinology Division.
Baraa RihawiAnesthesiology Department.
Joud AllouziDermatology Department, Aleppo University Hospital.
Mohammad I AllouziFaculty of Medicine.
Najwa AbdulrahmanPediatrics Department, Faculty of Medicine, University of Aleppo, Aleppo, Syria.
Manar AbdullahPediatrics Department, Faculty of Medicine, University of Aleppo, Aleppo, Syria.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

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.

Indexed as

case reportcystic fibrosishypochloremiahyponatremiaseizure

Identifiers

PMID37554905
PMCPMC10406084

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.