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Placental Floor Infarction Complicating the Pregnancy of a Fetus with Long-Chain 3-Hydroxyacyl-CoA Dehydrogenase (LCHAD) Deficiency

✍ Scribed by Dietrich Matern; Bahig M. Schehata; Prem Shekhawa; Arnold W. Strauss; Michael J. Bennett; Piero Rinaldo


Book ID
115639811
Publisher
Elsevier Science
Year
2001
Tongue
English
Weight
450 KB
Volume
72
Category
Article
ISSN
1096-7192

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## Abstract Long‐chain 3‐hydroxyacyl‐CoA dehydrogenase deficiency is an autosomal recessive disorder affecting mitochondrial fatty acid oxidation due to mutations in the __HADHA__ gene. We report on a 22‐month‐old child who was identified on expanded newborn screening with an abnormal acylcarnitine