Literature DB >> 22516080

Neurology of inherited glycosylation disorders.

Hudson H Freeze1, Erik A Eklund, Bobby G Ng, Marc C Patterson.   

Abstract

Congenital disorders of glycosylation comprise most of the nearly 70 genetic disorders known to be caused by impaired synthesis of glycoconjugates. The effects are expressed in most organ systems, and most involve the nervous system. Typical manifestations include structural abnormalities (eg, rapidly progressive cerebellar atrophy), myopathies (including congenital muscular dystrophies and limb-girdle dystrophies), strokes and stroke-like episodes, epileptic seizures, developmental delay, and demyelinating neuropathy. Patients can also have neurological symptoms associated with coagulopathies, immune dysfunction with or without infections, and cardiac, renal, or hepatic failure, which are common features of glycosylation disorders. The diagnosis of congenital disorder of glycosylation should be considered for any patient with multisystem disease and in those with more specific phenotypic features. Measurement of concentrations of selected glycoconjugates can be used to screen for many of these disorders, and molecular diagnosis is becoming more widely available in clinical practice. Disease-modifying treatments are available for only a few disorders, but all affected individuals benefit from early diagnosis and aggressive management.
Copyright © 2012 Elsevier Ltd. All rights reserved.

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Year:  2012        PMID: 22516080      PMCID: PMC3625645          DOI: 10.1016/S1474-4422(12)70040-6

Source DB:  PubMed          Journal:  Lancet Neurol        ISSN: 1474-4422            Impact factor:   44.182


  109 in total

1.  Cerebellar atrophy: an important feature of carbohydrate deficient glycoprotein syndrome type 1.

Authors:  H Antoun; N Villeneuve; A Gelot; S Panisset; C Adamsbaum
Journal:  Pediatr Radiol       Date:  1999-03

2.  Glycosylation type Ic disorder: idiopathic intracranial hypertension and retinal degeneration.

Authors:  M Y Kahook; N Mandava; J B Bateman; J A Thomas
Journal:  Br J Ophthalmol       Date:  2006-01       Impact factor: 4.638

Review 3.  Carbohydrate-deficient glycoprotein syndromes: peculiar group of new disorders.

Authors:  B A Hagberg; G Blennow; B Kristiansson; H Stibler
Journal:  Pediatr Neurol       Date:  1993 Jul-Aug       Impact factor: 3.372

4.  Myasthenic syndromes.

Authors:  M E Farrugia
Journal:  J R Coll Physicians Edinb       Date:  2011-03

5.  Glycomic analyses of mouse models of congenital muscular dystrophy.

Authors:  Stephanie H Stalnaker; Kazuhiro Aoki; Jae-Min Lim; Mindy Porterfield; Mian Liu; Jakob S Satz; Sean Buskirk; Yufang Xiong; Peng Zhang; Kevin P Campbell; Huaiyu Hu; David Live; Michael Tiemeyer; Lance Wells
Journal:  J Biol Chem       Date:  2011-04-01       Impact factor: 5.157

6.  Impaired glycosylation and cutis laxa caused by mutations in the vesicular H+-ATPase subunit ATP6V0A2.

Authors:  Uwe Kornak; Ellen Reynders; Aikaterini Dimopoulou; Jeroen van Reeuwijk; Bjoern Fischer; Anna Rajab; Birgit Budde; Peter Nürnberg; Francois Foulquier; Dirk Lefeber; Zsolt Urban; Stephanie Gruenewald; Wim Annaert; Han G Brunner; Hans van Bokhoven; Ron Wevers; Eva Morava; Gert Matthijs; Lionel Van Maldergem; Stefan Mundlos
Journal:  Nat Genet       Date:  2007-12-23       Impact factor: 38.330

7.  Conserved oligomeric Golgi complex subunit 1 deficiency reveals a previously uncharacterized congenital disorder of glycosylation type II.

Authors:  François Foulquier; Eliza Vasile; Els Schollen; Nico Callewaert; Tim Raemaekers; Dulce Quelhas; Jaak Jaeken; Philippa Mills; Bryan Winchester; Monty Krieger; Wim Annaert; Gert Matthijs
Journal:  Proc Natl Acad Sci U S A       Date:  2006-02-28       Impact factor: 11.205

8.  Congenital disorder of glycosylation type 1a: three siblings with a mild neurological phenotype.

Authors:  D Coman; J McGill; R MacDonald; D Morris; S Klingberg; J Jaeken; D Appleton
Journal:  J Clin Neurosci       Date:  2007-04-23       Impact factor: 1.961

Review 9.  Towards a therapy for phosphomannomutase 2 deficiency, the defect in CDG-Ia patients.

Authors:  Hudson H Freeze
Journal:  Biochim Biophys Acta       Date:  2009-09

Review 10.  Biological roles of oligosaccharides: all of the theories are correct.

Authors:  A Varki
Journal:  Glycobiology       Date:  1993-04       Impact factor: 4.313

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  71 in total

1.  N-glycosylation in regulation of the nervous system.

Authors:  Hilary Scott; Vladislav M Panin
Journal:  Adv Neurobiol       Date:  2014

2.  Early and lethal neurodegeneration with myasthenic and myopathic features: A new ALG14-CDG.

Authors:  David C Schorling; Simone Rost; Dirk J Lefeber; Lauren Brady; Clemens R Müller; Rudolf Korinthenberg; Mark Tarnopolsky; Carsten G Bönnemann; Richard J Rodenburg; Marianna Bugiani; Maria Beytia; Marcus Krüger; Marjo van der Knaap; Jan Kirschner
Journal:  Neurology       Date:  2017-07-21       Impact factor: 9.910

Review 3.  Neurological aspects of human glycosylation disorders.

Authors:  Hudson H Freeze; Erik A Eklund; Bobby G Ng; Marc C Patterson
Journal:  Annu Rev Neurosci       Date:  2015-04-02       Impact factor: 12.449

4.  DPAGT1 myasthenia and myopathy: genetic, phenotypic, and expression studies.

Authors:  Duygu Selcen; Xin-Ming Shen; Joan Brengman; Ying Li; Anthony A Stans; Eric Wieben; Andrew G Engel
Journal:  Neurology       Date:  2014-04-23       Impact factor: 9.910

5.  Sialic acids attached to N- and O-glycans within the Nav1.4 D1S5-S6 linker contribute to channel gating.

Authors:  Andrew R Ednie; Jean M Harper; Eric S Bennett
Journal:  Biochim Biophys Acta       Date:  2014-10-30

Review 6.  Understanding human glycosylation disorders: biochemistry leads the charge.

Authors:  Hudson H Freeze
Journal:  J Biol Chem       Date:  2013-01-17       Impact factor: 5.157

7.  A new congenital disorder of glycosylation caused by a mutation in SSR4, the signal sequence receptor 4 protein of the TRAP complex.

Authors:  Marie Estelle Losfeld; Bobby G Ng; Martin Kircher; Kati J Buckingham; Emily H Turner; Alexey Eroshkin; Joshua D Smith; Jay Shendure; Deborah A Nickerson; Michael J Bamshad; Hudson H Freeze
Journal:  Hum Mol Genet       Date:  2013-11-11       Impact factor: 6.150

8.  Limb girdle myasthenia with digenic RAPSN and a novel disease gene AK9 mutations.

Authors:  Ching-Wan Lam; Ka-Sing Wong; Ho-Wan Leung; Chun-Yiu Law
Journal:  Eur J Hum Genet       Date:  2016-12-14       Impact factor: 4.246

Review 9.  Mannose metabolism: more than meets the eye.

Authors:  Vandana Sharma; Mie Ichikawa; Hudson H Freeze
Journal:  Biochem Biophys Res Commun       Date:  2014-06-12       Impact factor: 3.575

10.  A homozygous PIGO mutation associated with severe infantile epileptic encephalopathy and corpus callosum hypoplasia, but normal alkaline phosphatase levels.

Authors:  Yoav Zehavi; Anja von Renesse; Etty Daniel-Spiegel; Yonatan Sapir; Luci Zalman; Ilana Chervinsky; Markus Schuelke; Rachel Straussberg; Ronen Spiegel
Journal:  Metab Brain Dis       Date:  2017-09-13       Impact factor: 3.584

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