A delayed diagnosis of familial chylomicronemia syndrome in an elderly patient: Clinical implications of late-onset disease

Recognition of characteristic biochemical profiles and family history is essential to avoid diagnostic delay and prevent irreversible pancreatic damage and malnutrition. Even in elderly patients, targeted therapy can substantially improve metabolic control and quality of life.

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Publication Details

Journal
Journal of clinical lipidology
Published
2025-12-19
DOI
https://doi.org/10.1016/j.jacl.2025.12.017
Primary Topic
Lipid metabolism and disorders
Type
article
Field-Weighted Citation Impact
0.00
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article

A delayed diagnosis of familial chylomicronemia syndrome in an elderly patient: Clinical implications of late-onset disease

Journal of clinical lipidology
Lipid metabolism and disorders
article

A delayed diagnosis of familial chylomicronemia syndrome in an elderly patient: Clinical implications of late-onset disease

article en

Abstract

Recognition of characteristic biochemical profiles and family history is essential to avoid diagnostic delay and prevent irreversible pancreatic damage and malnutrition. Even in elderly patients, targeted therapy can substantially improve metabolic control and quality of life.

Journal of clinical lipidologyVol. 20(3)
Federico II University Hospital (IT)
Zero hunger
Openalex Percentile: Top 32%
Lipid metabolism and disorders
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A delayed diagnosis of familial chylomicronemia syndrome in an elderly patient: Clinical implications of late-onset disease · Journal of clinical lipidology (2025) | TGRS Research Map | TGRS