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

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...

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Detalles Bibliográficos
Autores principales: Han, Lei, Qiang, Guangfeng, Yang, Lei, Kou, Rui, Li, Qiubo, Xin, Meiyun, Liu, Ruihan, Zhang, Zhengjun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Lippincott Williams & Wilkins 2022
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9371531/
https://www.ncbi.nlm.nih.gov/pubmed/35960041
http://dx.doi.org/10.1097/MD.0000000000029689

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9371531/
https://www.ncbi.nlm.nih.gov/pubmed/35960041
http://dx.doi.org/10.1097/MD.0000000000029689

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