What is another word for Galactokinase Deficiency Disease?
Pronunciation: [ɡˈalɐktˌɒkɪnˌe͡ɪs dɪfˈɪʃənsi dɪzˈiːz] (IPA) 
Galactokinase Deficiency Disease, also known as Galactosemia Type II, is a rare genetic disorder characterized by the body's inability to process galactose, a sugar found in milk and dairy products. Synonyms for this condition include Galactokinase Deficiency, Galactokinase Deficiency Disorder, and Galactose Kinase Deficiency. Symptoms of this disease may include cataracts, jaundice, liver enlargement, and intellectual disabilities if left untreated. It is important for individuals affected by this condition to follow a strict galactose-free diet to prevent potential complications. Early diagnosis and management are crucial in providing a better quality of life for those with Galactokinase Deficiency Disease.
