Literature DB >> 29443118

Neurometabolic disorders: Five new things.

Michèl A Willemsen1, Inga Harting1, Ron A Wevers1.   

Abstract

PURPOSE OF REVIEW: To present emerging issues in neurometabolic disorders, with an emphasis on the diagnostic workup of patients with suspected neurometabolic disorders and some future challenges in the care for these patients. RECENT
FINDINGS: Next-generation sequencing and next-generation metabolic screening increase the speed and yield of the diagnostic process in neurometabolic disorders. Furthermore, they deepen our insights into the underlying disease mechanisms. Care of adult patients with neurometabolic disorders is an expanding subspecialty, especially in internal medicine and neurology.
SUMMARY: We briefly discuss some novel genetic and biochemical laboratory techniques and changing insights in the molecular basis of disease, and illustrate the importance of MRI pattern recognition in the diagnostic process. Furthermore, we discuss gene therapy that is cautiously entering the field, and pay attention to the new field of (transition of) care for adult patients with inborn errors of metabolism.

Entities:  

Year:  2016        PMID: 29443118      PMCID: PMC5727707          DOI: 10.1212/CPJ.0000000000000266

Source DB:  PubMed          Journal:  Neurol Clin Pract        ISSN: 2163-0402


  46 in total

1.  GRID2 mutations span from congenital to mild adult-onset cerebellar ataxia.

Authors:  Marie Coutelier; Lydie Burglen; Emeline Mundwiller; Myriam Abada-Bendib; Diana Rodriguez; Sandra Chantot-Bastaraud; Christelle Rougeot; Marie-Anne Cournelle; Mathieu Milh; Annick Toutain; Delphine Bacq; Vincent Meyer; Alexandra Afenjar; Jean-François Deleuze; Alexis Brice; Delphine Héron; Giovanni Stevanin; Alexandra Durr
Journal:  Neurology       Date:  2015-04-03       Impact factor: 9.910

2.  Genome sequencing identifies major causes of severe intellectual disability.

Authors:  Christian Gilissen; Jayne Y Hehir-Kwa; Djie Tjwan Thung; Maartje van de Vorst; Bregje W M van Bon; Marjolein H Willemsen; Michael Kwint; Irene M Janssen; Alexander Hoischen; Annette Schenck; Richard Leach; Robert Klein; Rick Tearle; Tan Bo; Rolph Pfundt; Helger G Yntema; Bert B A de Vries; Tjitske Kleefstra; Han G Brunner; Lisenka E L M Vissers; Joris A Veltman
Journal:  Nature       Date:  2014-06-04       Impact factor: 49.962

3.  Autosomal dominant SCA5 and autosomal recessive infantile SCA are allelic conditions resulting from SPTBN2 mutations.

Authors:  Solaf M Elsayed; Raoul Heller; Michaela Thoenes; Maha S Zaki; Daniel Swan; Ezzat Elsobky; Christine Zühlke; Inga Ebermann; Gudrun Nürnberg; Peter Nürnberg; Hanno J Bolz
Journal:  Eur J Hum Genet       Date:  2013-07-10       Impact factor: 4.246

Review 4.  Diagnostic methods and recommendations for the cerebral creatine deficiency syndromes.

Authors:  Joseph F Clark; Kim M Cecil
Journal:  Pediatr Res       Date:  2014-12-18       Impact factor: 3.756

5.  Magnetic resonance imaging pattern recognition in hypomyelinating disorders.

Authors:  Marjan E Steenweg; Adeline Vanderver; Susan Blaser; Alberto Bizzi; Tom J de Koning; Grazia M S Mancini; Wessel N van Wieringen; Frederik Barkhof; Nicole I Wolf; Marjo S van der Knaap
Journal:  Brain       Date:  2010-10       Impact factor: 13.501

6.  Spastic paraplegia gene 7 in patients with spasticity and/or optic neuropathy.

Authors:  Stephan Klebe; Christel Depienne; Sylvie Gerber; Georges Challe; Mathieu Anheim; Perrine Charles; Estelle Fedirko; Elodie Lejeune; Julien Cottineau; Alfredo Brusco; Hélène Dollfus; Patrick F Chinnery; Cecilia Mancini; Xavier Ferrer; Guilhem Sole; Alain Destée; Jean-Michel Mayer; Bertrand Fontaine; Jérôme de Seze; Michel Clanet; Elisabeth Ollagnon; Philippe Busson; Cécile Cazeneuve; Giovanni Stevanin; Josseline Kaplan; Jean-Michel Rozet; Alexis Brice; Alexandra Durr
Journal:  Brain       Date:  2012-10       Impact factor: 13.501

7.  Brain white matter oedema due to ClC-2 chloride channel deficiency: an observational analytical study.

Authors:  Christel Depienne; Marianna Bugiani; Céline Dupuits; Damien Galanaud; Valérie Touitou; Nienke Postma; Carola van Berkel; Emiel Polder; Eleonore Tollard; Frédéric Darios; Alexis Brice; Christine E de Die-Smulders; Johannes S Vles; Adeline Vanderver; Graziella Uziel; Cengiz Yalcinkaya; Suzanna G Frints; Vera M Kalscheuer; Jan Klooster; Maarten Kamermans; Truus Em Abbink; Nicole I Wolf; Frédéric Sedel; Marjo S van der Knaap
Journal:  Lancet Neurol       Date:  2013-05-22       Impact factor: 44.182

8.  The Frequencies of Different Inborn Errors of Metabolism in Adult Metabolic Centres: Report from the SSIEM Adult Metabolic Physicians Group.

Authors:  S Sirrs; C Hollak; M Merkel; A Sechi; E Glamuzina; M C Janssen; R Lachmann; J Langendonk; M Scarpelli; T Ben Omran; F Mochel; M C Tchan
Journal:  JIMD Rep       Date:  2015-10-09

9.  Mutations in the SPG7 gene cause chronic progressive external ophthalmoplegia through disordered mitochondrial DNA maintenance.

Authors:  Gerald Pfeffer; Gráinne S Gorman; Helen Griffin; Marzena Kurzawa-Akanbi; Emma L Blakely; Ian Wilson; Kamil Sitarz; David Moore; Julie L Murphy; Charlotte L Alston; Angela Pyle; Jon Coxhead; Brendan Payne; George H Gorrie; Cheryl Longman; Marios Hadjivassiliou; John McConville; David Dick; Ibrahim Imam; David Hilton; Fiona Norwood; Mark R Baker; Stephan R Jaiser; Patrick Yu-Wai-Man; Michael Farrell; Allan McCarthy; Timothy Lynch; Robert McFarland; Andrew M Schaefer; Douglass M Turnbull; Rita Horvath; Robert W Taylor; Patrick F Chinnery
Journal:  Brain       Date:  2014-04-10       Impact factor: 13.501

10.  Spastic paraplegia and OXPHOS impairment caused by mutations in paraplegin, a nuclear-encoded mitochondrial metalloprotease.

Authors:  G Casari; M De Fusco; S Ciarmatori; M Zeviani; M Mora; P Fernandez; G De Michele; A Filla; S Cocozza; R Marconi; A Dürr; B Fontaine; A Ballabio
Journal:  Cell       Date:  1998-06-12       Impact factor: 41.582

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  2 in total

1.  Blood, urine and cerebrospinal fluid analysis in TH and AADC deficiency and the effect of treatment.

Authors:  Tessa Wassenberg; Ben P H Geurtz; Leo Monnens; Ron A Wevers; Michèl A Willemsen; Marcel M Verbeek
Journal:  Mol Genet Metab Rep       Date:  2021-04-26

Review 2.  Microcephaly in Neurometabolic Diseases.

Authors:  Wiktoria Kempińska; Karolina Korta; Magdalena Marchaj; Justyna Paprocka
Journal:  Children (Basel)       Date:  2022-01-11
  2 in total

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