Transitory tyrosinemia of newborn digital illustration

Transitory tyrosinemia of newborn Save


ICD-10 code: P74.5

Disease category: P74: Other transitory neonatal electrolyte and metabolic disturbances

Understanding Transitory Tyrosinemia of Newborn

Transitory tyrosinemia of newborn is a rare metabolic disorder that affects infants shortly after birth. It is characterized by elevated levels of the amino acid tyrosine in the blood. While the condition may cause concern for parents, it is typically a temporary condition that resolves on its own within a few weeks.

Here are some key points to know about transitory tyrosinemia of newborn:

  1. Causes: Transitory tyrosinemia of newborn occurs due to a deficiency of the enzyme responsible for breaking down tyrosine. This enzyme is not fully functional in newborns, leading to the accumulation of tyrosine in the blood.
  2. Symptoms: Infants with transitory tyrosinemia may exhibit symptoms such as yellowing of the skin and eyes (jaundice), poor weight gain, and a decreased appetite. However, these symptoms are often mild and tend to improve without medical intervention.
  3. Diagnosis: Transitory tyrosinemia is usually detected through routine newborn screening tests. Elevated levels of tyrosine in the blood may prompt further investigation to confirm the diagnosis.
  4. Management: In most cases, no specific treatment is required for transitory tyrosinemia. The condition typically resolves on its own as the baby's enzyme levels normalize. However, close monitoring by healthcare professionals is essential to ensure the baby's overall health.
  5. Dietary Considerations: Breastfeeding or providing formula milk is generally safe for infants with transitory tyrosinemia. However, in severe cases, a temporary restriction on dietary protein intake may be recommended to minimize the accumulation of tyrosine in the blood.

It is important to note that transitory tyrosinemia of newborn should not be confused with hereditary tyrosinemia, which is a more serious and chronic condition requiring long-term management.

While transitory tyrosinemia of newborn may cause worry for parents, understanding that it is usually a self-limiting condition can provide reassurance. Regular check-ups with healthcare professionals, adherence to recommended dietary guidelines, and providing a nurturing environment for the baby are key to managing this condition effectively.

Treatment of Transitory tyrosinemia of newborn:

Treatment Options for Transitory Tyrosinemia of Newborn

Transitory tyrosinemia of newborn is a rare metabolic disorder that affects infants shortly after birth. It is characterized by elevated levels of amino acid tyrosine in the blood, which can lead to various symptoms such as poor feeding, vomiting, and jaundice. While the condition usually resolves on its own within a few weeks...

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