Truninger_2006_Pancreas_32_215

Reference

Title : Recurrent acute and chronic pancreatitis in two brothers with familial chylomicronemia syndrome - Truninger_2006_Pancreas_32_215
Author(s) : Truninger K , Schmid PA , Hoffmann MM , Bertschinger P , Ammann RW
Ref : Pancreas , 32 :215 , 2006
Abstract :

The chylomicronemia syndrome is well recognized as a rare etiologic factor of acute pancreatitis; however, whether hypertriglyceridemia can cause chronic pancreatitis (CP) remains unclear. We describe the long-time course of 2 brothers with the familial chylomicronemia syndrome caused by identical compound heterozygous mutations in the lipoprotein lipase (LPL) gene with markedly reduced LPL activity. Other etiologic factors were excluded, including mutations in the PRSS1, SPINK1, and CFTR gene. Although both brothers had recurrent acute pancreatitis and the same LPL genotype, CP became evident in only one patient. Progression to CP was associated with a more severe disease course. Thus, the chylomicronemia syndrome may cause CP in the absence of other known causative factors, and similar to alcoholic and hereditary CP, a more severe disease course is associated with disease progression.

PubMedSearch : Truninger_2006_Pancreas_32_215
PubMedID: 16552344
Gene_locus related to this paper: human-LPL

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Citations formats

Truninger K, Schmid PA, Hoffmann MM, Bertschinger P, Ammann RW (2006)
Recurrent acute and chronic pancreatitis in two brothers with familial chylomicronemia syndrome
Pancreas 32 :215

Truninger K, Schmid PA, Hoffmann MM, Bertschinger P, Ammann RW (2006)
Pancreas 32 :215