Glossary for Ketoacidosis

Medical terms related to Ketoacidosis or mentioned in this section include:

• Abdominal symptoms: Symptoms affecting the abdomen or digestive tract
• Abnormal blood test symptoms: Abnormal results from diagnostic blood tests.
• Acidemia, propionic: An inherited genetic disorder where the body is incapable of processing some proteins and fats resulting in the accumulation of certain substances in the body which causes the symptoms of the condition. The condition can be life threatening.
• Acidosis: The accumulation of hydrogen ions or the depletion of the alkaline reserve in the body.
• Alcohol use: Use of alcohol (as a symptom)
• Biotinidase deficiency: A metabolic disorder where the body lacks the enzyme biotinidase needed to process the vitamin called biotin (vitamin H) into carboxylase enzymes.
• Blood symptoms: Symptoms affecting the blood and its blood cells.
• DEND syndrome: An inherited disorder characterized by developmental delay, epilepsy and diabetes.
• Diabetes: Symptoms similar to those of diabetes
• Diabetes-like symptoms: Symptoms similar to those of diabetes
• Diabetic Ketoacidosis: A metabolic acidosis that results from the accumulation of ketones when diabetes mellitus is poorly controlled
• Diabetic ketoacidosis: A metabolic acidosis that results from the accumulation of ketones when diabetes mellitus is poorly controlled
• Digestive symptoms: Any symptoms affecting the digestive tract.
• Forbes disease: A rare inherited glycogen storage disease caused by a deficiency of the enzyme amylo-1,6-glucosidase resulting in a build up of glycogen in the liver and muscles.
• Glycogen storage disease type 6: A rare, generally mild form of inherited glycogen storage disease where a deficiency of phosphorylase b kinase leads to hypoglycemia and accumulation of glycogen in the liver.
• Head symptoms: Symptoms affecting the head or brain
• Ketosis: The accumulation of ketone bodies in the body
• Lipoamide dehydrogenase deficiency: A very rare enzyme deficiency (dihydrolipoamide dehydrogenase) which can cause lactic acidosis. The age of onset and symptoms are variable.
• Malonic aciduria: A very rare genetic disorder where a deficiency of a particular enzyme (malonyl-CoA decarboxylase) impairs the body's ability to convert fatty acids into energy that can be used by muscles such as the heart muscle. Fatty acids also accumulate in the body as they are not metabolized.
• Marasmus: A form of malnutrition caused by a severe deficiency of both protein and calories
• Metabolic symptoms: Symptoms affecting the metabolic system.
• Muscle symptoms: Symptoms affecting the muscles of the body
• Muscle weakness: Weakness of the muscles or loss of tone
• Musculoskeletal symptoms: Symptoms affecting muscles or bones of the skeleton.
• Nerve symptoms: Symptoms affecting the nerves
• Propionic Acidemia: A condition which is characterized by the excess of propionic acid and glycine in the blood resulting in acidaemia
• Thinness: Underweight and thin
• Type 1 diabetes: Severe insulin-treated diabetes typically occurring in young people.
• Type 2 diabetes: Most common diabetes in adults, usually progressing slowly, mostly treated without insulin at diagnosis.

Conditions listing medical symptoms: Ketoacidosis:

The following list of conditions have 'Ketoacidosis' or similar listed as a symptom in our database. This computer-generated list may be inaccurate or incomplete. Always seek prompt professional medical advice about the cause of any symptom.

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Conditions listing medical complications: Ketoacidosis:

The following list of medical conditions have 'Ketoacidosis' or similar listed as a medical complication in our database.

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