Tag Archives: galactosemia
34(4) Update: Overview of Assessment of Nutrition Status for Children with Metabolic Disorders
Metabolic disorders are genetic (inherited) conditions. Previously identified through clinical symptoms (which were often catastrophic), advances in technology have allowed identification of metabolic disorders through newborn screening (NBS). Registered dietitians nutritionists (RDNs) are involved in the care of children with … Continue reading →
Posted in Nutrition-related Issues, Specific Conditions
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Tagged assessment, CSHCN, galactosemia, genetics, growth, intervention, mcad deficiency, medical food, metabolic disorders, newborn screening, nutrition management, pku, team members
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