Carbohydrate Metabolism Disorder Scholarly Journals
Carbohydrate metabolic disorders take many forms. The most common violations are recorded. Acquired or secondary carbohydrate metabolic disorders such as diabetic ketoacidosis, hyperosmolar coma and
hypoglycaemia affect the central nervous system. Many forms and variants of peripheral nerve disorders also occur in diabetes. Other carbohydrate metabolic disorders are rare metabolic disorders (i.e. genetic defects). Previously discovered defects that affect carbohydrate metabolism are inherited as autosomal recessive traits. Although many affected siblings can be identified in the genus, most affected individuals are the first to be identified in the family. Carbohydrate metabolic disorders are a group of metabolic disorders. The enzyme usually converts carbohydrates into glucose (a type of sugar). This disorder is inherited. New-borns are examined many of them who use blood tests. If one of these diseases has a family history, parents can carry out genetic testing to determine whether they have genes. Other genetic tests can show whether the foetus has a disorder or carry a
gene for the disorder. Treatment can include special diets, supplements, and medications. Some babies may also need additional care if complications arise. There is no cure for some disorders, but treatments can help with symptoms.
High Impact List of Articles
Relevant Topics in Medical