Lipodystrophy Report
Lipodystrophy
The term "Lipodystrophy" refers to a heterogeneous group of medical conditions characterized by the marked reduction or absence of subcutaneous adipose tissue. The first classification is based on the etiology, which can be genetic or acquired. Lipodystrophies of genetic origin are caused by mutations in specific genes that play key roles in the development and function of adipocytes.
4 genes analyzed
It is recommended if:
Genetic testing is useful for identifying subtypes of familial lipodystrophies and for at risk family members, especially for lipodystrophy subtypes associated with subtle physical phenotypes or those with high risk of morbidity and mortality.
List of main conditions:
- Lipodystrophy, congenital generalized, type 1
- Lipodystrophy, familial partial, type 2
Simple workflow
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