- What are common metabolic disorders?
- What is an example of a metabolic disease?
- What is a rare metabolic disorder?
- What doctor treats metabolic disorders?
- What are the 5 risk factors for metabolic syndrome?
- Are all metabolic disorders genetic?
- What is the most common inborn error of metabolism?
- How do I know if I have a metabolic disorder?
- Is Thyroid a metabolic disorder?
What are common metabolic disorders?
Examples include:Familial hypercholesterolemia.Gaucher disease.Hunter syndrome.Krabbe disease.Maple syrup urine disease.Metachromatic leukodystrophy.Mitochondrial encephalopathy, lactic acidosis, stroke-like episodes (MELAS)Niemann-Pick.More items…•.
What is an example of a metabolic disease?
Some affect the breakdown of amino acids, carbohydrates, or lipids. Another group, mitochondrial diseases, affects the parts of the cells that produce the energy. You can develop a metabolic disorder when some organs, such as your liver or pancreas, become diseased or do not function normally. Diabetes is an example.
What is a rare metabolic disorder?
Valinemia is a very rare metabolic disorder. It is characterized by elevated levels of the amino acid valine in the blood and urine caused by a deficiency of the enzyme valine transaminase. This enzyme is needed in the breakdown (metabolism) of valine.
What doctor treats metabolic disorders?
You’re likely to start by seeing your primary care provider. He or she may then refer you to a doctor who specializes in diabetes and other endocrine disorders (endocrinologist) or one who specializes in heart disease (cardiologist).
What are the 5 risk factors for metabolic syndrome?
The five risk factors are:increased blood pressure (greater than 130/85 mmHg)high blood sugar levels (insulin resistance)excess fat around the waist.high triglyceride levels.low levels of good cholesterol, or HDL.
Are all metabolic disorders genetic?
Inherited metabolic disorders are genetic conditions that result in metabolism problems. Most people with inherited metabolic disorders have a defective gene that results in an enzyme deficiency. There are hundreds of different genetic metabolic disorders, and their symptoms, treatments, and prognoses vary widely.
What is the most common inborn error of metabolism?
Inborn errors of metabolism most likely to cause acute decompensation in the neonate include certain forms of the tyrosinemia, organic acidemias, urea cycle defects, fatty acid oxidation defects, and galactosemia.
How do I know if I have a metabolic disorder?
Most of the disorders associated with metabolic syndrome don’t have obvious signs or symptoms. One sign that is visible is a large waist circumference. And if your blood sugar is high, you might notice the signs and symptoms of diabetes — such as increased thirst and urination, fatigue, and blurred vision.
Is Thyroid a metabolic disorder?
Hypothyroidism is one of the most important metabolic causes of reversible cognitive impairment. The term refers to thyroid underfunction within adults, which results in deficits of the thyroid hormones, thyroxine (T4) and triodothyronine (T3).