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Volume 59, Issue 4, Pages 463-467 (April 2010)


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Variable phenotypic expression of chylomicron retention disease in a kindred carrying a mutation of the Sara2 gene

Angelo B. Cefalùa1, Pier L. Calvob1, Davide Notoa, Maurizio Baldib, Vincenza Valentia, Pietro Lerrob, Fabio Tramutoc, Antonella Lezob, Isabella Morrad, Giovanna Cenacchie, Cristiana Barberab, Maurizio R. AvernaaCorresponding Author Informationemail address

Received 10 October 2008; accepted 8 July 2009. published online 21 October 2009.

Abstract 

Chylomicron retention disease is a recessive inherited disorder characterized by fat malabsorption and steatorrhea and is associated with failure to thrive in infancy. We describe a kindred carrying a mutation of Sara2 gene causing a chylomicron retention phenotype. The proband was a 5-month-old baby, born of consanguineous, apparently healthy parents from Morocco, with failure to thrive. There was a large quantity of fats in feces and malabsorption of fat-soluble vitamins. Intestinal biopsies showed a diffused enterocyte vacuolization with large cytosolic lipid droplets. Chylomicron retention disease or Anderson disease was hypothesized, and the Sara2 gene was analyzed by direct sequencing. Analysis of the Sara2 gene in the proband identified a 2-nucleotide homozygous deletion in exon 3 leading to a premature stop codon (c.75-76 del TG-L28fsX34). The father was heterozygous for the same mutation, whereas the proband's mother was homozygous, suggesting a variable phenotypic expression of the molecular defect. More studies are needed to understand the reasons of the phenotypic variability of the same molecular defect in the same family.

a Departmet of Clinical Medicine and Emerging Diseases, University of Palermo, I-90127 Palermo, Italy

b Department of Pediatric Gastroenterology, University of Turin, I-10126 Turin, Italy

c Department of Hygiene and Microbiology, University of Palermo, I-90127 Palermo, Italy

d Department of Pathology, Regina Margherita Hospital, Turin, I-10126 Turin, Italy

e Department of Pathology, Policlinico S. Orsola, I-40138 Bologna, Italy

Corresponding Author InformationCorresponding author. Tel.: +39 091 6552993; fax: +39 091 6552936.

1 These authors contributed equally to the work.

PII: S0026-0495(09)00351-5

doi:10.1016/j.metabol.2009.07.042


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