Recurrent acute fatty liver of pregnancy;Stéatose hépatique aiguë gravidique récidivante

Gastroenterologie Clinique et Biologique

Volumn 31, Issue 12, 2007, Pages 1135-1138

  Bacq, Yannick ^a   Assor, Philippe ^a   Gendrot, Chantal ^b   Perrotin, Franck ^b   Scotto, Béatrice ^a   Andres, Christian ^b,c  

^a SERVICE DE DERMATOLOGIE   (France)

^b CHU BRETONNEAU   (France)

^c UNIVERSITÉ DE TOURS   (France)

Author keywords

[No Author keywords available]

Indexed keywords

3 HYDROXYACYL COENZYME A DEHYDROGENASE; 3 HYDROXYACYL COENZYME A DEHYDROGENASE DELTA SUBUNIT; UNCLASSIFIED DRUG;

ABDOMINAL RADIOGRAPHY; ACUTE FATTY LIVER OF PREGNANCY; ADULT; ARTICLE; BLOOD CELL COUNT; CASE REPORT; CESAREAN SECTION; COMPUTER ASSISTED TOMOGRAPHY; DIAGNOSTIC PROCEDURE; ECHOGRAPHY; FATTY LIVER; FEMALE; GENE MUTATION; GESTATIONAL AGE; HUMAN; LIVER FUNCTION TEST; MATERNAL WELFARE; PREGNANCY DISORDER; RADIODIAGNOSIS; RECURRENCE RISK; RECURRENT DISEASE; THROMBOCYTOPENIA; VOMITING;

EID: 38049184793     PISSN: 03998320     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0399-8320(07)78351-3     Document Type: Article

References (32)

1. Sheehan HL. The pathology of acute yellow atrophy and delayed chloroform poisoning. J Obstet Gynaecol 1940;47:49-62.
2. Bernuau J, Degott C, Nouel O, Rueff B, Benhamou JP. Non-fatal acute fatty liver of pregnancy. Gut 1983;24:340-4.
3. Bacq Y. La stéatose hépatique aiguë gravidique. Gastroenterol Clin Biol 1997;21:109-15.
4. Ibdah JA, Yang Z, Bennett MJ. Liver disease in pregnancy and fetal fatty acid oxidation defects. Mol Genet Metab 2000;71:182-9.
5. Treem WR. Mitochondrial fatty acid oxidation and acute fatty liver of pregnancy. Semin Gastrointest Dis 2002;13:55-66.
6. Bacq Y, Constans T, Body G, Choutet P, Lamisse F. La stéatose hépatique aiguë gravidique. J Gynecol Obstet Biol Reprod (Paris) 1986;15:851-61.
7. Barton JR, Sibai BM, Mabie WC, Shanklin DR. Recurrent acute fatty liver of pregnancy. Am J Obstet Gynecol 1990;163:534-8.
8. Schoeman MN, Batey RG, Wilcken B. Recurrent acute fatty liver of pregnancy associated with a fatty-acid oxidation defect in the offspring. Gastroenterology 1991;100:544-8.
9. Meicler P, Bernuau J, Darai E, Morice P, Mansour F, Colau JC. Stéatose aiguë hépatique gravidique récidivante. Rev Fr Gynecol Obstet 1994;89:44-8.
10. MacLean MA, Cameron AD, Cumming GP, Murphy K, Mills P, Hilan KJ. Recurrence of acute fatty liver of pregnancy. Br J Obstet Gynaecol 1994;101:453-4.
11. Reyes H, Sandoval L, Wainstein A, Ribalta J, Donoso S, Smok G, et al. Acute fatty liver of pregnancy: a clinical study of 12 episodes in 11 patients. Gut 1994;35:101-6.
12. Visconti M, Manes G, Giannattasio F, Uomo G. Recurrence of acute fatty liver of pregnancy. J Clin Gastroenterol 1995;21:243-5.
13. Treem WR, Shoup ME, Hale DE, Bennett MJ, Rinaldo P, Millington DS, et al. Acute fatty liver of pregnancy, hemolysis, elevated liver enzymes, and low platelets syndrome, and long chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency. Am J Gastroenterol 1996;91:2293-300.
14. IJlst L, Ruiter JP, Hoovers JM, Jakobs ME, Wanders RJ. Common missense mutation G1528C in long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency. Characterization and expression of the mutant protein, mutation analysis on genomic DNA and chromosomal localization of the mitochondrial trifunctional protein alpha subunit gene. J Clin Invest 1996;98:1028-33.
15. Campillo B, Bernuau J, Witz MO, Lorphelin JM, Degott C, Rueff B, et al. Ultrasonography in acute fatty liver of pregnancy. Ann Intern Med 1986;105:383-4.
16. Goodacre RL, Hunter DJ, Millward S, Pirani M, Riddell RH. The diagnosis of acute fatty liver of pregnancy by computed tomography. J Clin Gastroenterol 1988;10:680-2.
17. McKee CM, Weir PE, Foster JH, Murnaghan GA, Callender ME. Acute fatty liver of pregnancy and diagnosis by computed tomography. Br Med J (Clin Res Ed) 1986;292:291-2.
18. Bacq Y. Acute fatty liver of pregnancy. Semin Perinatol 1998; 22:134-40.
19. Castro MA, Ouzounian JG, Colletti PM, Shaw KJ, Stein SM, Goodwin TM. Radiologic studies in acute fatty liver of pregnancy. A review of the literature and 19 new cases. J Reprod Med 1996;41:839-43.
20. Wilcken B, Leung KC, Hammond J, Kamath R, Leonard JV. Pregnancy and fetal long-chain 3-hydroxyacyl coenzyme A dehydrogenase deficiency. Lancet 1993;341:407-8.
21. Ibdah JA, Bennett MJ, Rinaldo P, Zhao Y, Gibson B, Sims HF, et al. A fetal fatty-acid oxidation disorder as a cause of liver disease in pregnant women. N Engl J Med 1999;340:1723-31.
22. Sims HF, Brackett JC, Powell CK, Treem WR, Hale DE, Bennett MJ, et al. The molecular basis of pediatric long chain 3-hydroxyacyl-CoA dehydrogenase deficiency associated with maternal acute fatty liver of pregnancy. Proc Natl Acad Sci USA 1995;92:841-5.
23. Bellig LL. Maternal acute fatty liver of pregnancy and the associated risk for long-chain 3-hydroxyacyl-coenzyme a dehydrogenase (LCHAD) deficiency in infants. Adv Neonatal Care 2004;4:26-32.
24. Yang Z, Yamada J, Zhao Y, Strauss AW, Ibdah JA. Prospective screening for pediatric mitochondrial trifunctional protein defects in pregnancies complicated by liver disease. JAMA 2002;288:2163-6.
25. Isaacs JD, Jr., Sims HF, Powell CK, Bennett MJ, Hale DE, Treem WR, et al. Maternal acute fatty liver of pregnancy associated with fetal trifunctional protein deficiency: molecular characterization of a novel maternal mutant allele. Pediatr Res 1996;40:393-8.
26. Yang Z, Zhao Y, Bennett MJ, Strauss AW, Ibdah JA. Fetal genotypes and pregnancy outcomes in 35 families with mitochondrial trifunctional protein mutations. Am J Obstet Gynecol 2002;187:715-20.
27. Shekhawat PS, Matern D, Strauss AW. Fetal fatty acid oxidation disorders, their effect on maternal health and neonatal outcome: impact of expanded newborn screening on their diagnosis and management. Pediatr Res 2005;57:78R-86R.
28. Mansouri A, Fromenty B, Durand F, Degott C, Bernuau J, Pessayre D. Assessment of the prevalence of genetic metabolic defects in acute fatty liver of pregnancy. J Hepatol 1996;25:781.
29. Maitra A, Domiati-Saad R, Yost N, Cunningham G, Rogers BB, Bennett MJ. Absence of the G1528C (E474Q) mutation in the alpha-subunit of the mitochondrial trifunctional protein in women with acute fatty liver of pregnancy. Pediatr Res 2002;51:658-61.
30. Fukushima K, Ueno Y, Inoue J, Kanno N, Nagasaki F, Mikami E, et al. Lack of common mutation in the alfa-subunit of the mitochondrial trifunctional protein and the polymorphism of CYP2E1 in three Japanese women with acute fatty liver of pregnancy/HELLP syndrome. Hepatol Res 2004;30:226-31.
31. Matern D, Hart P, Murtha AP, Vockley J, Gregersen N, Millington DS, et al. Acute fatty liver of pregnancy associated with short-chain acylcoenzyme A dehydrogenase deficiency. J Pediatr 2001;138:585-8.
32. Innes AM, Seargeant LE, Balachandra K, Roe CR, Wanders RJ, Ruiter JP, et al. Hepatic carnitine palmitoyltransferase I deficiency presenting as maternal illness in pregnancy. Pediatr Res 2000;47:43-5.