What is another word for Lysine Alpha Ketoglutarate Reductase Deficiency Disease?
Pronunciation: [lˈa͡ɪsa͡ɪn ˈalfə kˈɛtəɡlˌuːtɐɹˌe͡ɪt ɹɪdˈʌkte͡ɪs dɪfˈɪʃənsi dɪzˈiːz] (IPA) 
Lysine Alpha Ketoglutarate Reductase Deficiency Disease is a rare genetic disorder characterized by the absence or abnormality of the enzyme responsible for producing lysine alpha ketoglutarate reductase in the body. This deficiency leads to a range of symptoms, including developmental delays, intellectual disabilities, muscle weakness, and various metabolic abnormalities. Although there are no direct synonyms for this specific disease, it can also be referred to as LAKRDD, lysine reductase deficiency, or alpha ketoglutarate reductase deficiency disease. It is important to note that this condition requires specialized medical care and ongoing management to improve the quality of life for affected individuals.
