Successful pregnancy in severe methylmalonic acidaemia

Journal of Inherited Metabolic Disease

Volumn 22, Issue 7, 1999, Pages 788-794

  Wasserstein, M P ^a,b   Gaddipati, S ^b   Snyderman, S E ^a,b   Eddleman, K ^a,b   Desnick, R J ^a,b   Sansaricq, C ^a,b  

^a MOUNT SINAI MEDICAL CENTER   (United States)

^b MOUNT SINAI SCHOOL OF MEDICINE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

METHYLMALONYL COENZYME A MUTASE;

ADULT; ARTICLE; BLOOD LEVEL; CASE REPORT; CHRONIC KIDNEY FAILURE; CHRONIC PANCREATITIS; FEMALE; FETUS; HUMAN; INBORN ERROR OF METABOLISM; KETOACIDOSIS; METHYLMALONIC ACIDEMIA; ONSET AGE; OSTEOPENIA; PREGNANCY;

ACIDOSIS; ADULT; FEMALE; HUMANS; HYDROXOCOBALAMIN; INFANT, NEWBORN; MALE; METABOLISM, INBORN ERRORS; METHYLMALONIC ACID; METHYLMALONYL-COA MUTASE; PREGNANCY; PREGNANCY COMPLICATIONS; PREGNANCY OUTCOME; VITAMIN B 12;

EID: 0032845047     PISSN: 01418955     EISSN: None     Source Type: Journal    
DOI: 10.1023/A:1005597722237     Document Type: Article

References (17)

1. Arn PH, Hauser ER, Thomas GH, Herman G, Hess D, Brusilow SW (1990) Hyper-ammonemia in women with a mutation at the ornithine carbamoyltransferase locus - a cause of postpartum coma. N Engl J Med 322: 1652-1655.
2. Asrat T, Nageotte MP (1995) Renal disease. In James DK, Steer PJ, Weiner CP, Gonik B, eds. High Risk Pregnancy: Management Options. London: WB Saunders, 465-469.
3. Cabaniss, ML (1993) Fetal Monitoring Interpretation. Philadelphia: JB Lippincott.
4. Davison JM, Lindheimer MD (1994) Renal disorders. In Creasy RK, Resnik R, eds. Maternal-Fetal Medicine: Principles and Practice, 3rd edn. Philadelphia: WB Saunders, 847-854.
5. Diss E, Iams J, Reed N, Roe DS, Roe C (1995) Methylmalonic aciduria in pregnancy: a case report. Am J Obstet Gynecol 172: 1057-1059.
6. Fenton WA, Rosenberg LE (1995) Disorders of propionate and methylmalonate metabolism. In: Scriver CR, Beaudet Al, Sly WS, Valle D, eds. The Metabolic and Molecular Bases of Inherited Disease, 7th edn. New York: McGraw-Hill, 1423-1450.
7. Gittenger JW, (1996) Eye diseases. In: Bennett JC and Plum F, editors, Cecil Textbook of Medicine, 20th edn. Philadelphia: W. B. Saunders, 2178.
8. Grody WW, Chang RJ, Panagiotis NM, Matz D, Cederbaum SD (1994) Menstrual cycle and gonadal steroid effects on symptomatic hyperammoneaemia of urea-cycle-based and idiopathic aetiologies. J Inher Metab Dis 17: 566-574.
9. Grunewald S, Hinrichs F, Wendel U (1998) Pregnancy in a woman with maple syrup urine disease. J Inher Metab Dis 21: 89-94.
10. Hook EB (1981) Rates of chromosomal abnormalities at different maternal ages. Obstet Gynecol 58: 282.
11. Hook EB (1983) Chromosome abnormalities and spontaneous fetal death following amnio-centesis: further data and association with maternal age. Am J Hum Genet 35: 110.
12. Shih VE, Aubry RH, DeGrande G, Gursky SF, Tanaka K (1984) Maternal isovaleric acid-emia. J Pediatr 105: 77-78.
13. Slocum RH, Cummings JG (1991) Amino acid analysis of physiological samples. In Hommes F, ed. Techniques in Diagnostic Human Biochemical Genetics. New York: Wiley-Liss, 87-126.
14. Sweetman L (1991) Organic acid analysis. In Hommes F, ed. Techniques in Diagnostic Human Biochemical Genetics. New York: Wiley-Liss, 143-176.
15. Tropper PJ, Petrie RH (1987) Placental exchange. In The Human Placenta: Clinical Perspectives. Maryland: Aspen Publications, 199-206.
16. Van Calcar SC, Harding CO, Davidson SR, Barness LA, Wolff JA (1992) Case reports of successful pregnancy in women with maple syrup urine disease and propionic acidemia. Am J Med Genet 44: 641-646.
17. Worthington S, Christodoulou J, Wilcken B, Peat B (1996) Pregnancy and argininosuccinic aciduria. J Inher Metab Dis 19: 621-623.