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.