Lipodystrophy, congenital, generalized, type 1

Definition

The AGPAT2 gene encodes the enzyme that converts lysophosphatidic acid to phosphatidic acid in the triacylglycerol biosynthesis pathway; this step is critical for triglyceride storage in adipocytes. Mutations cause Berardinelli-Seip type 1, presenting from birth with near total absence of subcutaneous adipose tissue; severe hypertriglyceridemia, hepatic steatosis, and early insulin resistance are seen.

Gene/region examined

AGPAT2 - Exon 1, AGPAT2 - Exon 2, AGPAT2 - Exon 3, AGPAT2 - Exon 4, AGPAT2 - Exon 5, AGPAT2 - Exon 6, AGPAT2 - Exon 7

Method

Sequence analysis

Accepted sample types

EDTA blood, AF, CVS

Inheritance

Hereditary, autosomal recessive.

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