Frequently Asked Questions
Common Questions About Using ICD-10 Code E72.23 for Citrullinemia
What are the common symptoms of Citrullinemia?
Common symptoms of Citrullinemia include lethargy, irritability, vomiting, and developmental delays. Patients may also experience neurological symptoms due to elevated ammonia levels.
How is Citrullinemia diagnosed?
Citrullinemia is diagnosed through blood tests that measure levels of citrulline and ammonia, along with a thorough clinical evaluation and family history assessment.
What is the treatment for Citrullinemia?
Treatment for Citrullinemia typically involves dietary management to restrict protein intake, use of ammonia scavengers, and in severe cases, hospitalization for intravenous therapy.
Is Citrullinemia a hereditary condition?
Yes, Citrullinemia is an autosomal recessive genetic disorder, meaning it can be inherited from both parents who carry the mutated gene.
