Search...
Long-chain 3-hydroxyacyl-CoA dehydrogenase, or LCHAD, deficiency is a rare disorder of fatty acid metabolism that prevents the body from metabolizing certain types of fat. LCHAD deficiency usually first manifests in infants or young children as hypoketotic hypoglycemia, which is an episode of low blood sugar that can’t be compensated for by producing ketone bodies to obtain energy. Laboratory tests typically show low blood levels of glucose and ketone bodies, but the most important findings
By erica
Published
From the Pediatrics & Family Care community. 🧸 150K+ pros share on child and family care, including treatments and vaccines.
Posted in Chronic Pediatric Care. đź©ą Strategies for asthma, diabetes, and other chronic pediatric conditions.
75 views
6 likes