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Transitory disorders of carbohydrate metabolism specific to newborn Save


ICD-10 code: P70

Chapter: Certain conditions originating in the perinatal period

Transitory Disorders of Carbohydrate Metabolism Specific to Newborns

Newborn babies may have temporary difficulties in metabolizing carbohydrates, which can lead to various medical conditions. These disorders are typically self-limiting and do not require long-term medical intervention.

  1. Transient Hyperglycemia: This is a common condition in newborns, which typically occurs within the first few hours after birth. Transient hyperglycemia is characterized by a temporary increase in blood glucose levels, which usually normalize within a few days. The condition is often associated with maternal diabetes, delivery complications, or large birth weight babies.
  2. Transient Hypoglycemia: The opposite of transient hyperglycemia, transient hypoglycemia is characterized by low blood glucose levels in newborns. This condition is also common and typically occurs within the first few hours after birth. Transient hypoglycemia is usually caused by inadequate glucose production by the liver, decreased glycogen stores, or increased glucose utilization. The condition usually resolves within a few days.
  3. Galactosemia: This is a rare genetic disorder that affects the way a baby's body processes galactose, a type of sugar found in milk. Galactosemia can lead to severe health problems, including liver damage, intellectual disability, and developmental delays. Babies with galactosemia may experience jaundice, vomiting, lethargy, and poor feeding. Galactosemia is typically diagnosed through newborn screening tests and requires lifelong dietary restrictions.
  4. Fructose Intolerance: This is another rare genetic disorder that affects the way a baby's body processes fructose, a type of sugar found in fruits and some vegetables. Babies with fructose intolerance may experience vomiting, diarrhea, and failure to thrive. The condition can lead to liver and kidney damage if left untreated. Fructose intolerance is typically diagnosed through blood tests and requires lifelong dietary restrictions.

In conclusion, transitory disorders of carbohydrate metabolism specific to newborns are common and usually self-limiting. However, some rare genetic disorders like galactosemia and fructose intolerance require lifelong dietary restrictions to prevent severe health problems. It's important to consult a pediatrician if you notice any abnormal symptoms in your newborn baby.