Literature DB >> 29876767

The phenotype of adult versus pediatric patients with inborn errors of metabolism.

Jean-Marie Saudubray1, Fanny Mochel2,3,4,5.   

Abstract

Until recently, inborn errors of metabolism (IEM) were considered a pediatric specialty, as emphasized by the term "inborn," and the concept of adult onset IEM has only very recently reached the adult medical community. Still, an increasing number of adult onset IEM have now been recognized, as new metabolomics and molecular diagnostic techniques have become available. Here, we discuss possible mechanisms underlying phenotypic variability in adult versus children with IEM. Specifically, phenotypic severity and age of onset are expected to be modulated by differences in residual protein activity possibly driven by various genetic factors. Phenotypic variability may also occur in the context of similar protein expression, which suggests the intervention of environmental, ontogenic, and aging factors.

Entities:  

Keywords:  Aging; Environmental factors; Genetic factors; Inborn errors of metabolism; Ontogenic factors; Phenotypic variability

Mesh:

Year:  2018        PMID: 29876767     DOI: 10.1007/s10545-018-0209-9

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


  30 in total

1.  Ornithine aminotransferase deficiency: diagnostic difficulties in neonatal presentation.

Authors:  M A Cleary; L Dorland; T J de Koning; B T Poll-The; M Duran; R Mandell; V E Shih; R Berger; S E Olpin; G T N Besley
Journal:  J Inherit Metab Dis       Date:  2005       Impact factor: 4.982

2.  Somatic mosaicism for a PDHA1 mutation in a female with pyruvate dehydrogenase deficiency.

Authors:  Cheryl K Ridout; Ruth M Brown; John H Walter; Garry K Brown
Journal:  Hum Genet       Date:  2008-08-17       Impact factor: 4.132

3.  Thiamine responsive pyruvate dehydrogenase deficiency in an adult with peripheral neuropathy and optic neuropathy.

Authors:  F Sedel; G Challe; J-M Mayer; A Boutron; B Fontaine; J M Saudubray; M Brivet
Journal:  J Neurol Neurosurg Psychiatry       Date:  2008-07       Impact factor: 10.154

4.  Triheptanoin improves brain energy metabolism in patients with Huntington disease.

Authors:  Isaac Mawusi Adanyeguh; Daisy Rinaldi; Pierre-Gilles Henry; Samantha Caillet; Romain Valabregue; Alexandra Durr; Fanny Mochel
Journal:  Neurology       Date:  2015-01-07       Impact factor: 9.910

5.  Natural history, outcome, and treatment efficacy in children and adults with glutaryl-CoA dehydrogenase deficiency.

Authors:  Stefan Kölker; Sven F Garbade; Cheryl R Greenberg; James V Leonard; Jean-Marie Saudubray; Antonia Ribes; H Serap Kalkanoglu; Allan M Lund; Begoña Merinero; Moacir Wajner; Mónica Troncoso; Monique Williams; John H Walter; Jaume Campistol; Milagros Martí-Herrero; Melissa Caswill; Alberto B Burlina; Florian Lagler; Esther M Maier; Bernd Schwahn; Aysegul Tokatli; Ali Dursun; Turgay Coskun; Ronald A Chalmers; David M Koeller; Johannes Zschocke; Ernst Christensen; Peter Burgard; Georg F Hoffmann
Journal:  Pediatr Res       Date:  2006-04-26       Impact factor: 3.756

Review 6.  Triosephosphate isomerase deficiency: new insights into an enigmatic disease.

Authors:  Ferenc Orosz; Judit Oláh; Judit Ovádi
Journal:  Biochim Biophys Acta       Date:  2009-09-26

7.  A biotinidase Km variant causing late onset bilateral optic neuropathy.

Authors:  V T Ramaekers; T M Suormala; M Brab; R Duran; G Heimann; E R Baumgartner
Journal:  Arch Dis Child       Date:  1992-01       Impact factor: 3.791

Review 8.  GLUT1 deficiency syndrome: an update.

Authors:  D Gras; E Roze; S Caillet; A Méneret; D Doummar; T Billette de Villemeur; M Vidailhet; F Mochel
Journal:  Rev Neurol (Paris)       Date:  2013-11-20       Impact factor: 2.607

9.  Maple syrup urine disease: two different forms within a single family.

Authors:  J Frézal; O Amédée-Manesme; G Mitchell; S Heuertz; F Rey; J Rey; J M Saudubray
Journal:  Hum Genet       Date:  1985       Impact factor: 4.132

10.  Disease and patient characteristics in NP-C patients: findings from an international disease registry.

Authors:  Marc C Patterson; Eugen Mengel; Frits A Wijburg; Audrey Muller; Barbara Schwierin; Harir Drevon; Marie T Vanier; Mercé Pineda
Journal:  Orphanet J Rare Dis       Date:  2013-01-16       Impact factor: 4.123

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  5 in total

1.  Movement Disorders in Inherited Metabolic Diseases in Children.

Authors:  Arushi Gahlot Saini; Suvasini Sharma
Journal:  Ann Indian Acad Neurol       Date:  2020-05-09       Impact factor: 1.383

Review 2.  An overview of inborn errors of metabolism affecting the brain: from neurodevelopment to neurodegenerative disorders.

Authors:  Jean-Marie Saudubray; Angela Garcia-Cazorla
Journal:  Dialogues Clin Neurosci       Date:  2018-12       Impact factor: 5.986

3.  Education and training in adult metabolic medicine: Results of an international survey.

Authors:  Annalisa Sechi; Elisa Fabbro; Mirjam Langeveld; Annarita Tullio; Robin Lachmann; Fanny Mochel
Journal:  JIMD Rep       Date:  2019-06-21

Review 4.  2022 Overview of Metabolic Epilepsies.

Authors:  Birute Tumiene; Carlos R Ferreira; Clara D M van Karnebeek
Journal:  Genes (Basel)       Date:  2022-03-12       Impact factor: 4.096

5.  Comparison of Untargeted Metabolomic Profiling vs Traditional Metabolic Screening to Identify Inborn Errors of Metabolism.

Authors:  Ning Liu; Jing Xiao; Charul Gijavanekar; Kirk L Pappan; Kevin E Glinton; Brian J Shayota; Adam D Kennedy; Qin Sun; V Reid Sutton; Sarah H Elsea
Journal:  JAMA Netw Open       Date:  2021-07-01
  5 in total

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