TYPES
There are two types of inherited lipodystrophy, including:
Congenital generalized lipodystrophy (CGL). This is an uncommon genetic condition marked by a near-total loss of body fat and high muscularity, which is commonly present at birth or shortly after.
Familial partial lipodystrophy (FPL). This is a rare hereditary condition characterized by the loss of body fat from specific parts of the body over time.
SYMPTOMS
The two primary forms of inherited lipodystrophy have a lot of subtypes. They each have their particular symptoms. Its intensity also varies.
CGL. Babies appear extremely muscular since virtually little body fat is present. Most are bulging around a big belly button or hernia. They are proliferating and hungry. In areas, particularly on the neck, their flesh may be black, thick, and velvety; the trunk and the armpits of their body touch their legs.
FPL. The most prevalent type emerges around puberty. Children lose their legs, arms, and trunk fat while gaining fat in the chin, face, and neck. In folds and plasterings, they will acquire black, velvety skin. They may also have sensitivity to insulin and an expanded liver.