Severe hypertriglyceridemia as a cause of necrotizing pancreatitis in a pediatric patient with familial hyperchylomicronemia syndrome: A case report

Familial hyperchylomicronemia syndrome is a monogenic autosomal recessive disorder that causes severe and refractory hypertriglyceridemia. This uncommon condition is challenging to diagnose and treat and can lead to comorbidities such as acute pancreatitis. Although treatment options are limited in...

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Detalles Bibliográficos
Autores principales: Valenzuela-Vallejo, Laura, Meléndrez-Vásquez, Daniela, Durán-Ventura, Paola, Rivera-Nieto, Carolina, Lema, Adriana, Fernandez, Monica
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2022
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9274426/
https://www.ncbi.nlm.nih.gov/pubmed/35837325
http://dx.doi.org/10.1177/2050313X221109972

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9274426/
https://www.ncbi.nlm.nih.gov/pubmed/35837325
http://dx.doi.org/10.1177/2050313X221109972

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