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However, AFLP has been fatty acid molecule found associated in some cases with an abnormality of fatty-acid metabolism. This abnormality fatty acid molecule is a deficiency of the enzyme long-chain-3-hydroxyacyl-CoA dehydrogenease (LCHAD). The mother (and father) have 50% of normal LCHAD activity and the fetus has no LCHAD activity. The metabolic disease in the baby's liver apparently causes the fatty liver disease in the mother. In cases of AFLP fatty acid molecule due to LCHAD deficiency, there is a 25% (or greater) risk of AFLP in each pregnancy. Common Misspellings: acute fatty liver of pregnacy, acute fatty liver of pregancy, acute fatty liver of pregency, acute fatty liver of pregnanacy Search All of MedicineNet For: search help 1 Acute fatty liver of pregnancy Center | Next From the Doctors at MedicineNet.com
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