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A 1-month-old infant with chylomicronemia due to |
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Mo Kyung Jung, Juhyun Jin, Hyun Ok Kim, Ahreum Kwon, Hyun Wook Chae, Seok Jin Kang, Duk Hee Kim, Ho-Seong Kim | |
Ann Pediatr Endocrinol Metab. 2017;22(1):68-71. Published online March 31, 2017 DOI: https://doi.org/10.6065/apem.2017.22.1.68 |
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A 1-month-old infant with chylomicronemia due toGPIHBP1gene mutation treated by plasmapheresis Acquired Chylomicronemia Due to Autoantibodies Against GPIHBP1 Clinical and genetic features of 3 patients with familial chylomicronemia due to mutations in GPIHBP1 gene Familial chylomicronemia syndrome and response to medium-chain triglyceride therapy in an infant with novel mutations in GPIHBP1 Four-month-old male infant with generalized muscle weakness A nonsense germline mutation in the LPL gene in a 1-month-old infant: case report with review of literature Correction: A nonsense germline mutation in the LPL gene in a 1-month-old infant: case report with review of literature A very rare case of chylomicronemia revealed by cerebral thrombophlebitis in a 4-month-old infant A case of severe chylomicronaemia syndrome, in a patient with normal lipoprotein lipase activity, due to a previously unidentified mutation in the GPIHBP1 gene A novel mutation in GPIHBP1 causes familial chylomicronemia syndrome |