Prenatal diagnosis and therapy for a patient with vitamin B12-responsive methylmalonic acidaemia. 1995

H Soda, and T Ohura, and I Yoshida, and S Aramaki, and K Aoki, and T Inokuchi, and H Mikami, and K Narisawa
Department of Pediatrics and Child Health, Kurume University School of Medicine, Japan.

The prenatal therapy is described of a patient with vitamin B12-responsive methylmalonic acidaemia during the last 10 days of gestation with oral administration of vitamin B12 (20 mg/day) given to a mother did not normalize her urinary excretion of methylmalonic acid (MMA), which was 14.5 mmol/mol creatinine at 32 weeks of gestation. Before delivery, the mother was excreting 18.9 +/- 3.3 mmol MMA/mol creatinine (mean value at 7 days after vitamin B12 therapy), as well as at 32-37 weeks of gestation with no therapy. After birth, the level of MMA in the infant's urine was remarkably elevated (500-700 mmol/mol creatinine); the level of MMA in maternal urine decreased dramatically after delivery. Compared with two previous reports, the length of administration was not sufficient to reduce maternal MMA excretion. In future, the length of the therapy, route of administration and total dose of vitamin B12 to maintain an efficient level of vitamin B12 in an affected fetus should be considered.

UI MeSH Term Description Entries
D008661 Metabolism, Inborn Errors Errors in metabolic processes resulting from inborn genetic mutations that are inherited or acquired in utero. Inborn Errors of Metabolism,Metabolism Errors, Inborn,Error, Inborn Metabolism,Errors Metabolism, Inborn,Errors Metabolisms, Inborn,Errors, Inborn Metabolism,Inborn Errors Metabolism,Inborn Errors Metabolisms,Inborn Metabolism Error,Inborn Metabolism Errors,Metabolism Error, Inborn,Metabolism Inborn Error,Metabolism Inborn Errors,Metabolisms, Inborn Errors
D008764 Methylmalonic Acid A malonic acid derivative which is a vital intermediate in the metabolism of fat and protein. Abnormalities in methylmalonic acid metabolism lead to methylmalonic aciduria. This metabolic disease is attributed to a block in the enzymatic conversion of methylmalonyl CoA to succinyl CoA. Acid, Methylmalonic
D011247 Pregnancy The status during which female mammals carry their developing young (EMBRYOS or FETUSES) in utero before birth, beginning from FERTILIZATION to BIRTH. Gestation,Pregnancies
D011296 Prenatal Diagnosis Determination of the nature of a pathological condition or disease in the postimplantation EMBRYO; FETUS; or pregnant female before birth. Diagnosis, Prenatal,Fetal Diagnosis,Fetal Imaging,Fetal Screening,Intrauterine Diagnosis,Antenatal Diagnosis,Antenatal Screening,Diagnosis, Antenatal,Diagnosis, Intrauterine,Prenatal Screening,Antenatal Diagnoses,Antenatal Screenings,Diagnosis, Fetal,Fetal Diagnoses,Fetal Imagings,Fetal Screenings,Imaging, Fetal,Intrauterine Diagnoses,Prenatal Diagnoses,Prenatal Screenings,Screening, Antenatal,Screening, Fetal,Screening, Prenatal
D005260 Female Females
D005315 Fetal Diseases Pathophysiological conditions of the FETUS in the UTERUS. Some fetal diseases may be treated with FETAL THERAPIES. Embryopathies,Disease, Fetal,Diseases, Fetal,Embryopathy,Fetal Disease
D006801 Humans Members of the species Homo sapiens. Homo sapiens,Man (Taxonomy),Human,Man, Modern,Modern Man
D014805 Vitamin B 12 A cobalt-containing coordination compound produced by intestinal micro-organisms and found also in soil and water. Higher plants do not concentrate vitamin B 12 from the soil and so are a poor source of the substance as compared with animal tissues. INTRINSIC FACTOR is important for the assimilation of vitamin B 12. Cobalamin,Cyanocobalamin,Cobalamins,Eritron,Vitamin B12,B 12, Vitamin,B12, Vitamin

Related Publications

H Soda, and T Ohura, and I Yoshida, and S Aramaki, and K Aoki, and T Inokuchi, and H Mikami, and K Narisawa
August 1975, The New England journal of medicine,
H Soda, and T Ohura, and I Yoshida, and S Aramaki, and K Aoki, and T Inokuchi, and H Mikami, and K Narisawa
December 1990, The Journal of pediatrics,
H Soda, and T Ohura, and I Yoshida, and S Aramaki, and K Aoki, and T Inokuchi, and H Mikami, and K Narisawa
January 1996, Journal of inherited metabolic disease,
H Soda, and T Ohura, and I Yoshida, and S Aramaki, and K Aoki, and T Inokuchi, and H Mikami, and K Narisawa
January 1989, Journal of inherited metabolic disease,
H Soda, and T Ohura, and I Yoshida, and S Aramaki, and K Aoki, and T Inokuchi, and H Mikami, and K Narisawa
February 2006, Pediatric nephrology (Berlin, Germany),
H Soda, and T Ohura, and I Yoshida, and S Aramaki, and K Aoki, and T Inokuchi, and H Mikami, and K Narisawa
March 1980, The Journal of pediatrics,
H Soda, and T Ohura, and I Yoshida, and S Aramaki, and K Aoki, and T Inokuchi, and H Mikami, and K Narisawa
January 1995, Journal of inherited metabolic disease,
H Soda, and T Ohura, and I Yoshida, and S Aramaki, and K Aoki, and T Inokuchi, and H Mikami, and K Narisawa
January 1984, Journal of inherited metabolic disease,
H Soda, and T Ohura, and I Yoshida, and S Aramaki, and K Aoki, and T Inokuchi, and H Mikami, and K Narisawa
January 2005, Molecular genetics and metabolism,
H Soda, and T Ohura, and I Yoshida, and S Aramaki, and K Aoki, and T Inokuchi, and H Mikami, and K Narisawa
January 1982, Journal of inherited metabolic disease,
Copied contents to your clipboard!