Biochemical, clinical, and genetic characteristics of mexican patients with primary hypertriglyceridemia, including the first case of hyperchylomicronemia syndrome due to gpihbp1 deficiency

HIGHLIGHTS

• who: Perla Graciela Rodru00edguez-Gutiu00e9rrez and colleagues from the 00, Guadalajara, Jalisco, Mexico Doctorado en Humana, Centro Universitario Ciencias la Salud, Universidad Guadalajara have published the Article: Biochemical, Clinical, and Genetic Characteristics of Mexican Patients with Primary Hypertriglyceridemia, Including the First Case of Hyperchylomicronemia Syndrome Due to GPIHBP1 Deficiency, in the Journal: (JOURNAL) of 31/Oct/2022
• what: The authors report on the first Mexican patient with hyperchylomicronemia syndrome due to caused by three variants: p.R145 p.A154_G155insK and p.A154Rfs 152.
• how: Significant differences for several variables stood out when the . . .
  

   

  

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