Clinical Observation of a Child with Down Syndrome and Glucose and Galactose Malapsorbtion Syndrome

Abstract

The article deals with a clinical case of primary glucose and galactose malabsorption syndrome in a child with Down syndrome. Difficulty in diagnosis of glucose and galactose malabsorption syndrome in this observation is due to a combination of this disease with other genetic pathology. The article introduces pediatricians and family doctors to the possible comorbidities of various congenital nosological forms.

Keywords

• Down syndrome
• glucose and galactose malapsorbtion syndrome
• newborn
• diagnosis.