Literature DB >> 20830523

Treatment of cobalamin C (cblC) deficiency during pregnancy.

Catherine Brunel-Guitton1, Teresa Costa, Grant A Mitchell, Marie Lambert.   

Abstract

OBJECTIVE: To report the successful pregnancy of a woman with methylmalonic acidemia and hyperhomocysteinemia, cblC type [cobalamin C (cblC) deficiency] (MIM 277400).
METHOD: Retrospective chart review.
RESULTS: A 24-year-old woman presented at 14 weeks gestation with nausea, self-restricted protein diet, and weight loss. She had a past history of asymptomatic methylmalonic acidemia but had been lost to follow-up since the age of 15 years. Biochemical evaluation revealed combined methylmalonic acidemia and hyperhomocysteinemia. Complementation analysis confirmed cblC deficiency. One copy of the most common mutations in the MMACHC gene, c.271dupA, was identified. The women was treated from 15 weeks of gestation with a low protein diet (64 g/day) (1.1 g /kg of weight/day), L-carnitine (1 g per os 3 times daily to 3 g per os 3 times daily in the third trimester), aspirin (salicylic acid) 80 mg per day, folic acid 5 mg per day, and hydroxocobalamin 1 mg intramuscular every week to two times per week in the third trimester. The pregnancy was uneventful and the delivery at term. The newborn was healthy at delivery and at follow-up.
CONCLUSION: We report on the successful outcome of pregnancy in a treated woman with cblC disease. The pregnancy was uneventful for both fetus and mother with the delivery of a term healthy boy. There is a need for an international registry on the management and outcomes of pregnancy in women with inborn errors of metabolism.

Entities:  

Mesh:

Substances:

Year:  2010        PMID: 20830523     DOI: 10.1007/s10545-010-9202-7

Source DB:  PubMed          Journal:  J Inherit Metab Dis        ISSN: 0141-8955            Impact factor:   4.982


  24 in total

1.  Maternal pyridoxine non-responsive homocystinuria: the role of dietary treatment and anticoagulation.

Authors:  S Yap; C Barry-Kinsella; E R Naughten
Journal:  BJOG       Date:  2001-04       Impact factor: 6.531

2.  Adult-onset combined methylmalonic aciduria and homocystinuria (cblC).

Authors:  O A Bodamer; D S Rosenblatt; S H Appel; A L Beaudet
Journal:  Neurology       Date:  2001-04-24       Impact factor: 9.910

3.  Neurological and neuropathologic heterogeneity in two brothers with cobalamin C deficiency.

Authors:  J M Powers; D S Rosenblatt; R E Schmidt; A H Cross; J T Black; A B Moser; H W Moser; D J Morgan
Journal:  Ann Neurol       Date:  2001-03       Impact factor: 10.422

4.  Methylmalonic acidaemia: a rare metabolic disorder in pregnancy.

Authors:  O A Adeyemi; T Girish; S Mukhopadhyay; S A Olczak; Z Ahmed
Journal:  J Obstet Gynaecol       Date:  2004-11       Impact factor: 1.246

5.  Combined methylmalonic aciduria and homocystinuria (cblC): phenotype-genotype correlations and ethnic-specific observations.

Authors:  Chantal F Morel; Jordan P Lerner-Ellis; David S Rosenblatt
Journal:  Mol Genet Metab       Date:  2006-05-22       Impact factor: 4.797

6.  Low-dose aspirin in nulliparous women: safety of continuous epidural block and correlation between bleeding time and maternal-neonatal bleeding complications. National Institute of Child Health and Human Developmental Maternal-Fetal Medicine Network.

Authors:  B M Sibai; S N Caritis; E Thom; K Shaw; D McNellis
Journal:  Am J Obstet Gynecol       Date:  1995-05       Impact factor: 8.661

7.  Spectrum of MMACHC mutations in Italian and Portuguese patients with combined methylmalonic aciduria and homocystinuria, cblC type.

Authors:  Célia Nogueira; Chiara Aiello; Roberto Cerone; Esmeralda Martins; Ubaldo Caruso; Isabella Moroni; Cristiano Rizzo; Luísa Diogo; Elisa Leão; Fernando Kok; Federica Deodato; Maria Cristina Schiaffino; Sara Boenzi; Olivier Danhaive; Clara Barbot; Sílvia Sequeira; Mattia Locatelli; Filippo M Santorelli; Graziella Uziel; Laura Vilarinho; Carlo Dionisi-Vici
Journal:  Mol Genet Metab       Date:  2007-12-27       Impact factor: 4.797

8.  Methylmalonic aciduria in pregnancy: a case report.

Authors:  E Diss; J Iams; N Reed; D S Roe; C Roe
Journal:  Am J Obstet Gynecol       Date:  1995-03       Impact factor: 8.661

9.  Clinical heterogeneity in cobalamin C variant of combined homocystinuria and methylmalonic aciduria.

Authors:  G A Mitchell; D Watkins; S B Melançon; D S Rosenblatt; G Geoffroy; J Orquin; M B Homsy; L Dallaire
Journal:  J Pediatr       Date:  1986-03       Impact factor: 4.406

10.  Cobalamin disorder Cbl-C presenting with late-onset thrombotic microangiopathy.

Authors:  Johan L K Van Hove; Rita Van Damme-Lombaerts; Stephanie Grünewald; Heidi Peters; Boudewijn Van Damme; Jean-Pierre Fryns; Jozef Arnout; Ron Wevers; E Regula Baumgartner; Brian Fowler
Journal:  Am J Med Genet       Date:  2002-08-01
View more
  6 in total

Review 1.  Methylmalonic acidemia (MMA) in pregnancy: a case series and literature review.

Authors:  Donna B Raval; Melissa Merideth; Jennifer L Sloan; Nancy E Braverman; Robert L Conway; Irini Manoli; Charles P Venditti
Journal:  J Inherit Metab Dis       Date:  2015-01-08       Impact factor: 4.982

Review 2.  Combined methylmalonic acidemia and homocystinuria, cblC type. I. Clinical presentations, diagnosis and management.

Authors:  Nuria Carrillo-Carrasco; Randy J Chandler; Charles P Venditti
Journal:  J Inherit Metab Dis       Date:  2011-07-12       Impact factor: 4.982

Review 3.  Guidelines for diagnosis and management of the cobalamin-related remethylation disorders cblC, cblD, cblE, cblF, cblG, cblJ and MTHFR deficiency.

Authors:  Martina Huemer; Daria Diodato; Bernd Schwahn; Manuel Schiff; Anabela Bandeira; Jean-Francois Benoist; Alberto Burlina; Roberto Cerone; Maria L Couce; Angeles Garcia-Cazorla; Giancarlo la Marca; Elisabetta Pasquini; Laura Vilarinho; James D Weisfeld-Adams; Viktor Kožich; Henk Blom; Matthias R Baumgartner; Carlo Dionisi-Vici
Journal:  J Inherit Metab Dis       Date:  2016-11-30       Impact factor: 4.982

Review 4.  Impact of pregnancy on inborn errors of metabolism.

Authors:  Gisela Wilcox
Journal:  Rev Endocr Metab Disord       Date:  2018-03       Impact factor: 6.514

5.  Subcutaneous vitamin B12 administration using a portable infusion pump in cobalamin-related remethylation disorders: a gentle and easy to use alternative to intramuscular injections.

Authors:  Amelie S Lotz-Havla; Katharina J Weiß; Katharina A Schiergens; Theresa Brunet; Jürgen Kohlhase; Stephanie Regenauer-Vandewiele; Esther M Maier
Journal:  Orphanet J Rare Dis       Date:  2021-05-12       Impact factor: 4.123

6.  Clinical, phenotypic and genetic landscape of case reports with genetically proven inherited disorders of vitamin B12 metabolism: A meta-analysis.

Authors:  Arnaud Wiedemann; Abderrahim Oussalah; Nathalie Lamireau; Maurane Théron; Melissa Julien; Jean-Philippe Mergnac; Baptiste Augay; Pauline Deniaud; Tom Alix; Marine Frayssinoux; François Feillet; Jean-Louis Guéant
Journal:  Cell Rep Med       Date:  2022-06-27
  6 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.