Literature DB >> 28693988

Milder clinical and biochemical phenotypes associated with the c.482G>A (p.Arg161Gln) pathogenic variant in cobalamin C disease: Implications for management and screening.

Mohammed Almannai1, Ronit Marom1, Kristian Divin2, Fernando Scaglia1, V Reid Sutton1, William J Craigen1, Brendan Lee1, Lindsay C Burrage3, Brett H Graham4.   

Abstract

INTRODUCTION: Cobalamin C disease is a multisystemic disease with variable manifestations and age of onset. Genotype-phenotype correlations are well-recognized in this disorder. Here, we present a large cohort of individuals with cobalamin C disease, several of whom are heterozygous for the c.482G>A pathogenic variant (p.Arg161Gln). We compared clinical characteristics of individuals with this pathogenic variant to those who do not have this variant. To our knowledge, this study represents the largest single cohort of individuals with the c.482G>A (p.Arg161Gln) pathogenic variant.
METHODS: A retrospective chart review of 27 individuals from 21 families with cobalamin C disease who are followed at our facility was conducted.
RESULTS: 13 individuals (48%) are compound heterozygous with the c.482G>A (p.Arg161Gln) on one allele and a second pathogenic variant on the other allele. Individuals with the c.482G>A (p.Arg161Gln) pathogenic variant had later onset of symptoms and easier metabolic control. Moreover, they had milder biochemical abnormalities at presentation which likely contributed to the observation that 4 individuals (31%) in this group were missed by newborn screening.
CONCLUSION: The c.482G>A (p.Arg161Gln) pathogenic variant is associated with milder disease. These individuals may not receive a timely diagnosis as they may not be identified on newborn screening or because of unrecognized, late onset symptoms. Despite the milder presentation, significant complications can occur, especially if treatment is delayed.
Copyright © 2017 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Cobalamin C; Genotype-phenotype; Hydroxocobalamin; Late-onset; R161Q

Mesh:

Substances:

Year:  2017        PMID: 28693988      PMCID: PMC5612879          DOI: 10.1016/j.ymgme.2017.06.011

Source DB:  PubMed          Journal:  Mol Genet Metab        ISSN: 1096-7192            Impact factor:   4.797


  41 in total

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

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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
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2.  Elevated methylmalonic acidemia (MMA) screening markers in Hispanic and preterm newborns.

Authors:  Gang Peng; Christina A de Fontnouvelle; Gregory M Enns; Tina M Cowan; Hongyu Zhao; Curt Scharfe
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3.  Next Generation Sequencing in Newborn Screening in the United Kingdom National Health Service.

Authors:  Julia C van Campen; Elizabeth S A Sollars; Rebecca C Thomas; Clare M Bartlett; Antonio Milano; Matthew D Parker; Jennifer Dawe; Peter R Winship; Gerrard Peck; Darren Grafham; Richard J Kirk; James R Bonham; Anne C Goodeve; Ann Dalton
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4.  Peripheral Nervous System Involvement in Late-Onset Cobalamin C Disease?

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6.  Expanded Newborn Screening in Italy Using Tandem Mass Spectrometry: Two Years of National Experience.

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7.  Adolescent/adult-onset homocysteine remethylation disorders characterized by gait disturbance with/without psychiatric symptoms and cognitive decline: a series of seven cases.

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8.  Variable phenotypes and outcomes associated with the MMACHC c.609G>A homologous mutation: long term follow-up in a large cohort of cases.

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