Literature DB >> 32991969

Congenital disorders of glycosylation: Still "hot" in 2020.

Nina Ondruskova1, Anna Cechova1, Hana Hansikova1, Tomas Honzik2, Jaak Jaeken3.   

Abstract

BACKGROUND: Congenital disorders of glycosylation (CDG) are inherited metabolic diseases caused by defects in the genes important for the process of protein and lipid glycosylation. With the ever growing number of the known subtypes and discoveries regarding the disease mechanisms and therapy development, it remains a very active field of study. SCOPE OF REVIEW: This review brings an update on the CDG-related research since 2017, describing the novel gene defects, pathobiomechanisms, biomarkers and the patients' phenotypes. We also summarize the clinical guidelines for the most prevalent disorders and the current therapeutical options for the treatable CDG. MAJOR
CONCLUSIONS: In the majority of the 23 new CDG, neurological involvement is associated with other organ disease. Increasingly, different aspects of cellular metabolism (e.g., autophagy) are found to be perturbed in multiple CDG. GENERAL SIGNIFICANCE: This work highlights the recent trends in the CDG field and comprehensively overviews the up-to-date clinical recommendations.
Copyright © 2020 Elsevier B.V. All rights reserved.

Entities:  

Keywords:  CDG; Clinical guidelines; Glycosylation; Novel phenotypes; Pathobiomechanism; Therapy

Mesh:

Substances:

Year:  2020        PMID: 32991969     DOI: 10.1016/j.bbagen.2020.129751

Source DB:  PubMed          Journal:  Biochim Biophys Acta Gen Subj        ISSN: 0304-4165            Impact factor:   3.770


  20 in total

1.  Active site variants in STT3A cause a dominant type I congenital disorder of glycosylation with neuromusculoskeletal findings.

Authors:  Matthew P Wilson; Alejandro Garanto; Filippo Pinto E Vairo; Bobby G Ng; Wasantha K Ranatunga; Marina Ventouratou; Melissa Baerenfaenger; Karin Huijben; Christian Thiel; Angel Ashikov; Liesbeth Keldermans; Erika Souche; Sandrine Vuillaumier-Barrot; Thierry Dupré; Helen Michelakakis; Agata Fiumara; James Pitt; Susan M White; Sze Chern Lim; Lyndon Gallacher; Heidi Peters; Daisy Rymen; Peter Witters; Antonia Ribes; Blai Morales-Romero; Agustí Rodríguez-Palmero; Diana Ballhausen; Pascale de Lonlay; Rita Barone; Mirian C H Janssen; Jaak Jaeken; Hudson H Freeze; Gert Matthijs; Eva Morava; Dirk J Lefeber
Journal:  Am J Hum Genet       Date:  2021-10-14       Impact factor: 11.025

2.  Development and Validation of a Prognostic Classifier Based on Lipid Metabolism-Related Genes for Breast Cancer.

Authors:  Nan Wang; Yuanting Gu; Lin Li; Jiangrui Chi; Xinwei Liu; Youyi Xiong; Chaochao Zhong
Journal:  J Inflamm Res       Date:  2022-06-14

3.  Neurological Consequences of Congenital Disorders of Glycosylation.

Authors:  Justyna Paprocka
Journal:  Adv Neurobiol       Date:  2023

4.  ALG13 X-linked intellectual disability: New variants, glycosylation analysis, and expanded phenotypes.

Authors:  Hind Alsharhan; Miao He; Andrew C Edmondson; Earnest J P Daniel; Jie Chen; Tyhiesia Donald; Somayeh Bakhtiari; David J Amor; Elizabeth A Jones; Grace Vassallo; Marie Vincent; Benjamin Cogné; Wallid Deb; Arend H Werners; Sheng C Jin; Kaya Bilguvar; John Christodoulou; Richard I Webster; Katherine R Yearwood; Bobby G Ng; Hudson H Freeze; Michael C Kruer; Dong Li; Kimiyo M Raymond; Elizabeth J Bhoj; Andrew K Sobering
Journal:  J Inherit Metab Dis       Date:  2021-03-26       Impact factor: 4.750

Review 5.  Oligomannose-Type Glycan Processing in the Endoplasmic Reticulum and Its Importance in Misfolding Diseases.

Authors:  Taiki Kuribara; Kiichiro Totani
Journal:  Biology (Basel)       Date:  2022-01-27

6.  ALG1-CDG Caused by Non-functional Alternative Splicing Involving a Novel Pathogenic Complex Allele.

Authors:  Carlos Alberto González-Domínguez; Moisés O Fiesco-Roa; Samuel Gómez-Carmona; Anke Paula Ingrid Kleinert-Altamirano; Miao He; Earnest James Paul Daniel; Kimiyo M Raymond; Melania Abreu-González; Sandra Manrique-Hernández; Ana González-Jaimes; Roberta Salinas-Marín; Carolina Molina-Garay; Karol Carrillo-Sánchez; Luis Leonardo Flores-Lagunes; Marco Jiménez-Olivares; Anallely Muñoz-Rivas; Mario E Cruz-Muñoz; Matilde Ruíz-García; Hudson H Freeze; Héctor M Mora-Montes; Carmen Alaez-Verson; Iván Martínez-Duncker
Journal:  Front Genet       Date:  2021-09-09       Impact factor: 4.599

Review 7.  Chondrodysplasias With Multiple Dislocations Caused by Defects in Glycosaminoglycan Synthesis.

Authors:  Johanne Dubail; Valérie Cormier-Daire
Journal:  Front Genet       Date:  2021-06-16       Impact factor: 4.599

8.  Non-functional alternative splicing caused by a Latino pathogenic variant in a case of PMM2-CDG.

Authors:  C A González-Domínguez; C E Villarroel; M Rodríguez-Morales; S Manrique-Hernández; A González-Jaimes; F Olvera-Rodriguez; K Beutelspacher; C Molina-Garay; K Carrillo-Sánchez; L L Flores-Lagunes; M Jiménez-Olivares; A Muñoz-Rivas; M E Cruz-Muñoz; H M Mora-Montes; R Salinas-Marín; C Alaez-Verson; I Martínez-Duncker
Journal:  Mol Genet Metab Rep       Date:  2021-07-02

9.  Should patients with Phosphomannomutase 2-CDG (PMM2-CDG) be screened for adrenal insufficiency?

Authors:  Anna Čechová; Tomáš Honzík; Andrew C Edmondson; Can Ficicioglu; Mercedes Serrano; Rita Barone; Pascale De Lonlay; Manuel Schiff; Peter Witters; Christina Lam; Marc Patterson; Mirian C H Janssen; Joana Correia; Dulce Quelhas; Jolanta Sykut-Cegielska; Horacio Plotkin; Eva Morava; Kyriakie Sarafoglou
Journal:  Mol Genet Metab       Date:  2021-06-11       Impact factor: 4.204

10.  Liver Involvement in Congenital Disorders of Glycosylation: A Systematic Review.

Authors:  Rossella Colantuono; Elisa D'Acunto; Daniela Melis; Pietro Vajro; Hudson H Freeze; Claudia Mandato
Journal:  J Pediatr Gastroenterol Nutr       Date:  2021-10-01       Impact factor: 3.288

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