How Do You Care For A Child With Metabolic Disorders?
Metabolic disorders are inherited problems that affect a child’s ability to digest carbohydrates or the amino acids in proteins. Doctors must diagnose infants with metabolic disorders and offer nutritional intervention soon after birth, as untreated metabolic disorders can cause severe side effects, such as neurological impairments. Most hospitals screen newborns for metabolic disorders allowing proper dietary management right away. Restrict the phenylalanine intake of children diagnosed with hyperphenylalaninemia metabolic disorders. The child can choose low-protein pastas, breads and cookies provided by dietary specialty companies for this purpose. Offer a low tyrosine diet and restrict the phenylalanine in the diet of children with tyrosinemia metabolic disorders. Patients with some types of tyrosinemia require vitamin D supplementation to prevent a fatal onset of rickets. Reduce the amino acids leucine, isoleucine and valine for children with maple syrup urine diseases. Parents can
