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Plasma exchange therapy for familial chylomicronemia syndrome in infant: A case report

12 Aug 2022

Abstract excerpt

INTRODUCTION: Familial chylomicronemia syndrome (FCS) is a rare genetic disease. FCS usually manifests by the age of 10 years, and 25% of cases of FCS occur during infancy. Here we present a case of FCS in a male infant and summarize our experiences on the diagnosis and therapy of this case. PATIENT CONCERNS: A male infant aged 1 month and 8 days had recurrent hematochezia and hyperchylomicronemia. DIAGNOSIS: FCS...

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PMID: 35960041
DOI: 10.1097/md.0000000000029689

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