What is another word for lecithin cholesterol acyltransferase deficiency?
Pronunciation: [lˈɛsɪθˌɪn kəlˈɛstəɹˌɒl ɐkˈɪltɹɐnsfˌɜːɹe͡ɪz dɪfˈɪʃənsi] (IPA) 
Lecithin cholesterol acyltransferase deficiency is a rare metabolic disorder that affects the body's ability to metabolize cholesterol. This disorder is also known as LCAT deficiency. It is characterized by a deficiency in the enzyme Lecithin cholesterol acyltransferase, which is involved in the processing of cholesterol and fats in the body.
There are several synonyms for Lecithin cholesterol acyltransferase deficiency. These include Familial LCAT Deficiency, Fish Eye Disease, and LCAT Deficiency Syndrome. These terms are often used interchangeably to describe the same disorder.
Familial LCAT Deficiency is the most common synonym used to describe LCAT deficiency. This term emphasizes the genetic aspect of the disorder and indicates that it can be inherited from one or both parents.
Fish Eye Disease is another synonym for LCAT deficiency. This term comes from the appearance of the eyes in some individuals with the disorder.
