Frequently Asked Questions
Common Questions About Using ICD-10 Code E71.310 for Long chain/very long chain acyl CoA dehydrogenase deficiency
What are the common symptoms of Long chain/very long chain acyl CoA dehydrogenase deficiency?
Common symptoms include hypoglycemia, fatigue, weakness, and recurrent metabolic crises, particularly during fasting or illness.
How is Long chain/very long chain acyl CoA dehydrogenase deficiency diagnosed?
Diagnosis is typically made through clinical evaluation, metabolic testing showing elevated long-chain fatty acids, and genetic testing for ACADL gene mutations.
What is the treatment for Long chain/very long chain acyl CoA dehydrogenase deficiency?
Treatment includes dietary management to avoid fasting, supplementation with medium-chain triglycerides, and intravenous dextrose during metabolic crises.
Is Long chain/very long chain acyl CoA dehydrogenase deficiency hereditary?
Yes, it is an autosomal recessive genetic disorder, meaning both parents must carry the gene mutation for a child to be affected.
