Literature DB >> 26608391

A Highly Diverse Portrait: Heterogeneity of Neuropsychological Profiles in cblC Defect.

Jenny Bellerose1,2, Mathilde Neugnot-Cerioli1,2, Karine Bédard3,4, Catherine Brunel-Guitton5, Grant A Mitchell2,3, Luis H Ospina6, Miriam H Beauchamp7,8.   

Abstract

Cobalamin C is a rare inborn disorder of metabolism that results in multisystemic abnormalities, including progressive visual deficits. Although the cellular pathophysiology of cblC is a field of active study, little attention has been dedicated to documenting the cognitive consequences of the defect. The neuropsychological assessment of nine individuals aged between 23 months and 24 years was conducted to establish cognitive profiles. Results reveal a marked heterogeneity, with intellectual functioning ranging from extremely low to average, and cognitive difficulties (e.g., attention) evidenced even in those who are not intellectually disabled. Central nervous system abnormalities and multisystem disease are likely to be major contributing factors to the observed cognitive impairments, with the presence of visual deficits constituting an additional impediment to normal cognitive development. This study underscores the importance of conducting in-depth neuropsychological assessments in individuals with cblC, the results of which may be particularly helpful for clinical management, guidance toward rehabilitation services, and educational/vocational planning.

Entities:  

Year:  2015        PMID: 26608391      PMCID: PMC5059201          DOI: 10.1007/8904_2015_517

Source DB:  PubMed          Journal:  JIMD Rep        ISSN: 2192-8304


  25 in total

1.  Cobalamin (Cbl) C/D deficiency: clinical, neurophysiological and neuroradiologic findings in 14 cases.

Authors:  R Biancheri; R Cerone; M C Schiaffino; U Caruso; E Veneselli; M V Perrone; A Rossi; R Gatti
Journal:  Neuropediatrics       Date:  2001-02       Impact factor: 1.947

2.  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

3.  Long-term visual outcome of methylmalonic aciduria and homocystinuria, cobalamin C type.

Authors:  Robert Gizicki; Marie-Claude Robert; Lilianne Gómez-López; Jaqueline Orquin; Jean-Claude Decarie; Grant A Mitchell; Marie-Sylvie Roy; Luis H Ospina
Journal:  Ophthalmology       Date:  2013-10-11       Impact factor: 12.079

4.  Early-onset combined methylmalonic aciduria and homocystinuria: neuroradiologic findings.

Authors:  A Rossi; R Cerone; R Biancheri; R Gatti; M C Schiaffino; C Fonda; E Zammarchi; P Tortori-Donati
Journal:  AJNR Am J Neuroradiol       Date:  2001-03       Impact factor: 3.825

5.  Cobalamin C mutation (methylmalonic aciduria and homocystinuria) in adolescence. A treatable cause of dementia and myelopathy.

Authors:  S Shinnar; H S Singer
Journal:  N Engl J Med       Date:  1984-08-16       Impact factor: 91.245

Review 6.  High cognitive outcome in an adolescent with mut- methylmalonic acidemia.

Authors:  L Varvogli; G M Repetto; S E Waisbren; H L Levy
Journal:  Am J Med Genet       Date:  2000-04-03

7.  Identification of the gene responsible for methylmalonic aciduria and homocystinuria, cblC type.

Authors:  Jordan P Lerner-Ellis; Jamie C Tirone; Peter D Pawelek; Carole Doré; Janet L Atkinson; David Watkins; Chantal F Morel; T Mary Fujiwara; Emily Moras; Angela R Hosack; Gail V Dunbar; Hana Antonicka; Vince Forgetta; C Melissa Dobson; Daniel Leclerc; Roy A Gravel; Eric A Shoubridge; James W Coulton; Pierre Lepage; Johanna M Rommens; Kenneth Morgan; David S Rosenblatt
Journal:  Nat Genet       Date:  2005-11-27       Impact factor: 38.330

Review 8.  Cobalamin C defect: natural history, pathophysiology, and treatment.

Authors:  Diego Martinelli; Federica Deodato; Carlo Dionisi-Vici
Journal:  J Inherit Metab Dis       Date:  2010-07-15       Impact factor: 4.982

9.  High prevalence of structural heart disease in children with cblC-type methylmalonic aciduria and homocystinuria.

Authors:  Laurie E Profitlich; Brian Kirmse; Melissa P Wasserstein; George A Diaz; Shubhika Srivastava
Journal:  Mol Genet Metab       Date:  2009-08-12       Impact factor: 4.797

10.  Cobalamin C defect presenting with isolated pulmonary hypertension.

Authors:  Francesca G Iodice; Luca Di Chiara; Sara Boenzi; Chiara Aiello; Lidia Monti; Paola Cogo; Carlo Dionisi-Vici
Journal:  Pediatrics       Date:  2013-06-10       Impact factor: 7.124

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  3 in total

1.  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

2.  Parenteral hydroxocobalamin dose intensification in five patients with different types of early onset intracellular cobalamin defects: Clinical and biochemical responses.

Authors:  Emmanuel Scalais; Elise Osterheld; Christine Geron; Charlotte Pierron; Ronit Chafai; Vincent Schlesser; Patricia Borde; Luc Regal; Hilde Laeremans; Koen L I van Gassen; L Bert van den Heuvel; Linda De Meirleir
Journal:  JIMD Rep       Date:  2019-07-01

Review 3.  Neurodevelopmental and neuropsychiatric disorders in cobalamin C disease: a case report and review of the literature.

Authors:  Minh G Nguyen; Lauren Tronick; Faraz Modirian; Rebecca Mardach; Aaron D Besterman
Journal:  Cold Spring Harb Mol Case Stud       Date:  2022-03-24
  3 in total

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