What is another word for hexokinase deficiency?
Pronunciation: [hˈɛksəkˌɪne͡ɪs dɪfˈɪʃənsi] (IPA) 
Hexokinase deficiency is a genetic disorder that affects a person's ability to metabolize glucose. The condition is also referred to as hexokinase 1 deficiency or HK1 deficiency. Other synonyms for this disorder include Glucose Phosphorylation Deficiency, GK Deficiency, Hexokinase 1 Disorder and HK-1D. People with this disorder may experience episodes of hypoglycemia, a condition characterized by low blood sugar levels. This can cause a lack of energy, confusion, and even seizures. While there may not be a cure for this condition, certain treatments, such as a low-carbohydrate diet, may help manage its symptoms. In some cases, medication may also be prescribed.
