Özet:

The disease of glucose galactose malabsorption is a disorder of the sodium-dependent glucose carrier system, which has an autosomal resessive genetic transition characteristic. In this disease, where glucose and galactosone are not absorbed in the thin stomach mucus, the baby usually develops abundant, hydrated diarrhoea and hyernatremic dehydration. In cases where diagnosis and treatment cannot be placed, the death can be seen, while the diarrhea can be stopped with the proper diet where glucose and galactosone are removed from the diet, the normal development of the baby can be achieved. In our article, 2 facts diagnosed with glucose galactose malabsorption in the newborn period were presented in order to emphasize that the disease is rarely identified as a cause of chronic diarrhea in the newborn period.

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