FAMILIAL HYPERTRIGLYCERIDEMIAS Meaning and
Definition
-
Familial Hypertriglyceridemias refers to a group of inherited metabolic disorders characterized by abnormally high levels of triglycerides in the bloodstream. Triglycerides are a type of fat (lipid) that play a crucial role in storing energy. They are synthesized in the liver and are derived from dietary fats.
In individuals with Familial Hypertriglyceridemias, an underlying genetic mutation affects the metabolism and regulation of triglycerides, resulting in their excessive accumulation. This condition can be categorized into different types based on the specific gene mutations involved and the severity of symptoms.
Symptoms of Familial Hypertriglyceridemias may vary depending on the type, but common manifestations include elevated levels of triglycerides (usually exceeding 500 mg/dL), pancreatitis (inflammation of the pancreas), xanthomas (yellowish deposits of fat under the skin), and hepatosplenomegaly (enlargement of the liver and spleen). Additionally, affected individuals may experience recurrent abdominal pain, which could be an indicator of acute pancreatitis.
Treatment for Familial Hypertriglyceridemias usually involves lifestyle modifications to manage the condition and reduce the risk of complications. This includes adopting a low-fat, low-calorie diet, regular physical activity, and weight management. Medications, such as fibrates or omega-3 fatty acid derivatives, may be prescribed to further control triglyceride levels. In severe cases, plasmapheresis, a procedure to selectively remove blood lipids, might be recommended. Genetic counseling may be beneficial to individuals with Familial Hypertriglyceridemias and their families for understanding inheritance patterns and assessing the risk of passing on the condition to future generations.
Common Misspellings for FAMILIAL HYPERTRIGLYCERIDEMIAS
- damilial hypertriglyceridemias
- camilial hypertriglyceridemias
- vamilial hypertriglyceridemias
- gamilial hypertriglyceridemias
- tamilial hypertriglyceridemias
- ramilial hypertriglyceridemias
- fzmilial hypertriglyceridemias
- fsmilial hypertriglyceridemias
- fwmilial hypertriglyceridemias
- fqmilial hypertriglyceridemias
- fanilial hypertriglyceridemias
- fakilial hypertriglyceridemias
- fajilial hypertriglyceridemias
- famulial hypertriglyceridemias
- famjlial hypertriglyceridemias
- famklial hypertriglyceridemias
- famolial hypertriglyceridemias
- fam9lial hypertriglyceridemias
- fam8lial hypertriglyceridemias
- famikial hypertriglyceridemias
Etymology of FAMILIAL HYPERTRIGLYCERIDEMIAS
The term "Familial Hypertriglyceridemias" is a medical term used to describe a group of genetic disorders characterized by elevated levels of triglycerides in the blood.
Etymology:
- "Familial" comes from the Latin word "familia", which means family or household. In the context of medical terminology, "familial" refers to conditions or traits that are inherited within families due to genetic factors.
- "Hyper" is a Greek prefix meaning excessive or above normal.
- "Triglyceridemias" is a combination of two components. "Triglycerides" are a type of fat molecule found in the bloodstream, and "emias" is a suffix derived from the Greek word "haima", meaning blood.
