Congenital disorders of glycosylation (CDG): it's (nearly) all in it!
- PMID: 21384229
- DOI: 10.1007/s10545-011-9299-3
Congenital disorders of glycosylation (CDG): it's (nearly) all in it!
Abstract
Congenital disorders of glycosylation (CDG) is a booming class of metabolic diseases. Its number has increased nearly fourfold (to 45) since 2003, the year of the Komrower lecture, entitled 'Congenital disorders of glycosylation CDG): It's all in it!'. This paper presents an overview of recently discovered CDG and CDG phenotypes, of a diagnostic approach, of (the lack of) treatment, of CDG genetics, of a novel CDG nomenclature and classification, and of some future directions in the CDG field.
Similar articles
-
Diseases of glycosylation beyond classical congenital disorders of glycosylation.Biochim Biophys Acta. 2012 Sep;1820(9):1306-17. doi: 10.1016/j.bbagen.2012.02.001. Epub 2012 Feb 9. Biochim Biophys Acta. 2012. PMID: 22343051 Review.
-
Congenital disorders of glycosylation. Part I. Defects of protein N-glycosylation.Acta Biochim Pol. 2013;60(2):151-61. Epub 2013 May 31. Acta Biochim Pol. 2013. PMID: 23730680 Review.
-
On the nomenclature of congenital disorders of glycosylation (CDG).J Inherit Metab Dis. 2008 Dec;31(6):669-72. doi: 10.1007/s10545-008-0983-x. Epub 2008 Oct 24. J Inherit Metab Dis. 2008. PMID: 18949576
-
Laboratory diagnosis of congenital disorders of glycosylation type I by analysis of transferrin glycoforms.Mol Diagn Ther. 2007;11(5):303-11. doi: 10.1007/BF03256251. Mol Diagn Ther. 2007. PMID: 17963418 Review.
-
How to find and diagnose a CDG due to defective N-glycosylation.J Inherit Metab Dis. 2011 Aug;34(4):849-52. doi: 10.1007/s10545-011-9370-0. Epub 2011 Jul 8. J Inherit Metab Dis. 2011. PMID: 21739167 Free PMC article. No abstract available.
Cited by
-
Natural history of three late-diagnosed classic Galactosemia patients.Mol Genet Metab Rep. 2024 Jan 23;38:101057. doi: 10.1016/j.ymgmr.2024.101057. eCollection 2024 Mar. Mol Genet Metab Rep. 2024. PMID: 38469096 Free PMC article.
-
PIGO-CDG: A case study with a new genotype, expansion of the phenotype, literature review, and nosological considerations.JIMD Rep. 2023 Sep 20;64(6):424-433. doi: 10.1002/jmd2.12396. eCollection 2023 Nov. JIMD Rep. 2023. PMID: 37927489 Free PMC article.
-
Congenital disorders of glycosylation (CDG): state of the art in 2022.Orphanet J Rare Dis. 2023 Oct 19;18(1):329. doi: 10.1186/s13023-023-02879-z. Orphanet J Rare Dis. 2023. PMID: 37858231 Free PMC article. Review.
-
Defining the phenotype of PGAP3-congenital disorder of glycosylation; a review of 65 cases.Mol Genet Metab. 2023 Nov;140(3):107688. doi: 10.1016/j.ymgme.2023.107688. Epub 2023 Aug 23. Mol Genet Metab. 2023. PMID: 37647829 Review.
-
Synthesis, Processing, and Function of N-Glycans in N-Glycoproteins.Adv Neurobiol. 2023;29:65-93. doi: 10.1007/978-3-031-12390-0_3. Adv Neurobiol. 2023. PMID: 36255672 Review.
References
Publication types
MeSH terms
LinkOut - more resources
Full Text Sources
Other Literature Sources
Medical
