Hypochlorhydria is a deficiency of hydrochloric acid in the stomach. A low level of this acid can affect your digestion and cause symptoms, such as bloating, indigestion, and nausea. Stomach Signs and symptoms. Hunter syndrome may present with a wide variety of phenotypes. It has traditionally been categorized as either "mild" or "severe" depending on the presence of central nervous system symptoms, but this is an oversimplification. Patients with "attenuated" or "mild" forms of the disease may still have significant health issues. 4. Fatigue. You may find that you’re feeling constantly tired throughout the day, or after you eat your meals. Carbohydrate intolerance can affect your energy levels due to blood sugar spikes and lows caused by not absorbing carbs efficiently, or by not being able to use their energy effectively. Kwashiorkor is a form of acute malnutrition that occurs due to protein deficiency. It can cause swelling, loss of appetite, lack of muscle and fat tissues, and more. Kwashiorkor is a serious Anemia is a condition in which the number of red blood cells may be inadequate or the cells may be abnormal in size or color. There may be multiple causes, including excessive blood loss, cell destruction, or improper cell formation. Several trace mineral deficiencies can result in anemia. 82lSK. Pyruvate carboxylase deficiency is an inherited disorder that causes lactic acid to accumulate in the blood. [2] High levels of these substances can damage the body's organs and tissues, particularly in the nervous system. Pyruvate carboxylase deficiency is a rare condition, with an estimated incidence of 1 in 250,000 births worldwide. Signs of Vitamin B1 deficiency. Vitamin B1, also known as thiamine, is necessary for the diet of cats. Its deficiency will show symptoms such as anorexia, vomiting along with neurological signs, including dilated pupils, impaired vision, vestibular signs, ataxia, seizures, and tremors. Glycogen storage disease (GSD) is a rare condition that changes the way the body uses and stores glycogen, a form of sugar or glucose. Glycogen is a main source of energy for the body. Glycogen is stored in the liver. When the body needs more energy, certain proteins called enzymes break down glycogen into glucose. Introduction. The disorders in this chapter can be divided into disorders of carbohydrate absorption and transmembrane transport, galactose and fructose metabolism, glycolysis, glycogen synthesis, glycogenolysis and gluconeogenesis (Nomenclature Table). Most are inherited according to an autosomal recessive trait. This section covers the following signs and symptoms of metabolic diseases of muscle: Cardiac care Exercise intolerance Muscle weakness Myogloburina Respiratory care Cardiac care People with debrancher enzyme deficiency, carnitine deficiency and acid maltase deficiency may develop significant heart problems. In the case of primary carnitine deficiency, the only symptom may be heart failure

deficiency signs and symptoms of carbohydrates