Lipidoses are heredity disorders, passed from parents to their children, characterized by defects of the digestive system that impair the way the body uses fat from the diet.
Some lipidoses disorders can be controlled with changes in the diet, medications, or enzyme supplements.
Arthur Sawitsky has written: 'Reticuloendothelial disorders: the lipidoses' -- subject(s): Lipidoses
In most cases of lipidoses, the body does not produce a certain enzyme or chemical.
Genetic testing can be used, in some cases, to identify the defective gene causing lipidoses.
Some lipidoses disorders may cause death in childhood or contribute to a shortened life expectancy.
Some lipidoses disorders become apparent shortly after the infant is born; in others, symptoms may not develop until adulthood.
People with lipidoses are born without the genetic codes needed to tell their bodies how to complete a particular part of the fat digestion process.
For most of the lipidoses, diagnosis is suspected based on the symptoms and family history.
Blood tests, urine tests, and tissue tests can be used to confirm a diagnosis of lipidoses.
Couples who have family histories of genetic defects can undergo genetic testing and counseling to see if they are at risk for having a child with one of the lipidoses disorders.