What is Berardinelli-Seip congenital lipodystrophy, type 1?
What is Berardinelli-Seip congenital lipodystrophy, type 1?
- Berardinelli-Seip congenital lipodystrophy, type 1: A rare genetic disorder characterized by early-onset diabetes mellitus, loss of body fat, serious insulin resistance, high blood triglycerides and fatty liver. Type 1 is distinguished from type 2 by the origin of the genetic defect. Type 1 is caused by a defect on the AGPAT2 gene on chromosome 9q34.3. Type 1 seems to be less severe with some cases of type 2 resulting in premature death which can occur as early as the first year of life. Type 2 also involves mental retardation which is not seen in type 1.
Berardinelli-Seip congenital lipodystrophy, type 1: Introduction
How serious is Berardinelli-Seip congenital lipodystrophy, type 1?
Complications of Berardinelli-Seip congenital lipodystrophy, type 1:
see complications of Berardinelli-Seip congenital lipodystrophy, type 1
What are the symptoms of Berardinelli-Seip congenital lipodystrophy, type 1?
Symptoms of Berardinelli-Seip congenital lipodystrophy, type 1:
see symptoms of Berardinelli-Seip congenital lipodystrophy, type 1
Complications of Berardinelli-Seip congenital lipodystrophy, type 1:
see complications of Berardinelli-Seip congenital lipodystrophy, type 1
Berardinelli-Seip congenital lipodystrophy, type 1: Testing
Diagnostic testing: see tests for Berardinelli-Seip congenital lipodystrophy, type 1.
Misdiagnosis: see misdiagnosis and Berardinelli-Seip congenital lipodystrophy, type 1.
How is it treated?
Treatments for Berardinelli-Seip congenital lipodystrophy, type 1:
see treatments for Berardinelli-Seip congenital lipodystrophy, type 1
Name and Aliases of Berardinelli-Seip congenital lipodystrophy, type 1
Main name of condition: Berardinelli-Seip congenital lipodystrophy, type 1
Other names or spellings for Berardinelli-Seip congenital lipodystrophy, type 1:
CGL1, BSCL1, lipodystrophy, Berardinelli-Seip congenital, type 1, Brunzell syndrome [AGPAT2-related]
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