Literature DB >> 29274890

Molybdenum cofactor deficiency type A: Prenatal monitoring using MRI.

Charlotte M A Lubout1, Terry G J Derks1, Linda Meiners2, Jan Jaap Erwich3, Klasien A Bergman4, Roelineke J Lunsing5, Guenter Schwarz6, Alex Veldman7, Francjan J van Spronsen8.   

Abstract

Molybdenum cofactor deficiency type A (MoCD-A) is an inborn error of metabolism presenting early after birth with severe seizures. Recently, experimental substitution treatment with cyclic pyranopterin monophosphate (cPMP) has become available. Because prenatal data is scarce, we report data of prenatal Magnetic Resonance Imaging (MRI) in two cases with MoCD-A demonstrating signs of possible early brain injury. Prenatal MRI can be used for monitoring in MoCD-A to guide decision-making in timing of delivery.
Copyright © 2017 European Paediatric Neurology Society. Published by Elsevier Ltd. All rights reserved.

Entities:  

Keywords:  Cyclic pyranopterin monophosphate; MoCD-A; Molybdenum cofactor deficiency type A; cPMP; prenatal Magnetic Resonance Imaging

Mesh:

Year:  2017        PMID: 29274890     DOI: 10.1016/j.ejpn.2017.11.006

Source DB:  PubMed          Journal:  Eur J Paediatr Neurol        ISSN: 1090-3798            Impact factor:   3.140


  3 in total

1.  Mild phenotype in Molybdenum cofactor deficiency: A new patient and review of the literature.

Authors:  Barbara Scelsa; Serena Gasperini; Andrea Righini; Maria Iascone; Valeria G Brazzoduro; Pierangelo Veggiotti
Journal:  Mol Genet Genomic Med       Date:  2019-03-21       Impact factor: 2.183

2.  The effect of dietary protein restriction in a case of molybdenum cofactor deficiency with MOCS1 mutation.

Authors:  Yu Abe; Yu Aihara; Wakaba Endo; Hiroshi Hasegawa; Kimiyoshi Ichida; Mitsugu Uematsu; Shigeo Kure
Journal:  Mol Genet Metab Rep       Date:  2021-02-01

3.  Molybdenum Cofactor Deficiency: Mega Cisterna Magna in Two Consecutive Pregnancies and Review of the Literature.

Authors:  M C Alonzo Martínez; E Cazorla; E Cánovas; K Anniuk; A E Cores; A M Serrano
Journal:  Appl Clin Genet       Date:  2020-01-30
  3 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.