Some lipidoses disorders can be controlled with changes in the diet, medications, or enzyme supplements.
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.
Arthur Sawitsky has written: 'Reticuloendothelial disorders: the lipidoses' -- subject(s): Lipidoses
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.
Genetic testing can be used, in some cases, to identify the defective gene causing 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.
In most cases of lipidoses, the body does not produce a certain enzyme or chemical.
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.
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Some autosomal disorders in humans that are controlled by dominant alleles include Huntington's disease, Marfan syndrome, and neurofibromatosis type 1. These disorders are expressed when an individual inherits a single copy of the mutated gene from one parent.
For most of the lipidoses, diagnosis is suspected based on the symptoms and family history.
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