Питание детей раннего возраста при наследственных болезнях обмена веществ

Ольга Пантелеймоновна Романенко

Ольга Пантелеймоновна Романенко 1 St. Petersburg State Public Health Institution “Diagnostic center (medical genetic)”; 2 North-Western State Medical University named after I.I. Mechnikov 194044, St. Petersburg, Tobolsk, st., 5; Saint-Petersburg, 191015, Kirochnaya ul. 41

Keywords: diet therapy, hereditary metabolic diseases, phenylketonuria, leucinosis, organic aciduria, homocystinuria, galactosemia, fructosemia

Abstract

The lecture presents the basic principles of diet therapy of hereditary metabolic diseases. Effective diet therapy is developed for phenylketonuria (fku), leucinosis (urine smell maple syrup), organic aciduria (methylmalonic, propionic, isovalerian and glutaric), some forms of homocystinuria, galactosemia, fructosemia, etc.Recommendations for the diet, are excluded products.The effectiveness of a combination of diet and drug therapy is shown.

Infant feeding in hereditary metabolic diseases

Abstract