Literature DB >> 29229467

Renal involvement in PMM2-CDG, a mini-review.

Ruqaiah Altassan1, Peter Witters2, Zubaida Saifudeen3, Dulce Quelhas4, Jaak Jaeken2, Elena Levtchenko2, David Cassiman5, Eva Morava6.   

Abstract

Phosphomannomutase 2 deficiency (PMM2-CDG) is the most common N-linked glycosylation disorder. The majority of patients present with a multisystem phenotype, including central nervous system involvement, hepatopathy, gastrointestinal and cardiac symptoms, endocrine dysfunction and abnormal coagulation. Renal abnormalities including congenital malformations and altered renal function are part of the multisystem manifestations of congenital disorders of glycosylation. We reviewed the literature on 933 patients with molecularly and/or enzymatically confirmed PMM2 deficiency to evaluate the incidence of renal involvement in PMM2-CDG. Renal abnormalities were reported in 56 patients. Congenital abnormalities were present in 41 out of these 55. Cystic kidney and mild proteinuria were the most common findings. One of the most severe renal manifestations, congenital nephrotic syndrome, was detected in 6 children. Renal manifestations were not associated with the presence of specific PMM2 alleles. This review summarizes the reported renal abnormalities in PMM2-CDG and draws attention to the pathophysiological impact of abnormal glycosylation on kidney structure and function.
Copyright © 2017 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  CDG; Cystic kidney; Glycosylation; PMM2-CDG; Proteinuria

Mesh:

Substances:

Year:  2017        PMID: 29229467     DOI: 10.1016/j.ymgme.2017.11.012

Source DB:  PubMed          Journal:  Mol Genet Metab        ISSN: 1096-7192            Impact factor:   4.797


  7 in total

1.  Podocyte-Specific Sialylation-Deficient Mice Serve as a Model for Human FSGS.

Authors:  Kristina M Niculovic; Linda Blume; Henri Wedekind; Elina Kats; Iris Albers; Stephanie Groos; Markus Abeln; Jessica Schmitz; Esther Beuke; Jan H Bräsen; Anette Melk; Mario Schiffer; Birgit Weinhold; Anja K Münster-Kühnel
Journal:  J Am Soc Nephrol       Date:  2019-04-30       Impact factor: 10.121

2.  Vascular ring anomaly in a patient with phosphomannomutase 2 deficiency: A case report and review of the literature.

Authors:  Zhen Qian; Jef Van den Eynde; Stephane Heymans; Luc Mertens; Eva Morava
Journal:  JIMD Rep       Date:  2020-08-19

Review 3.  Perspectives on Glycosylation and Its Congenital Disorders.

Authors:  Bobby G Ng; Hudson H Freeze
Journal:  Trends Genet       Date:  2018-03-29       Impact factor: 11.639

4.  Clinical, biochemical and molecular phenotype of congenital disorders of glycosylation: long-term follow-up.

Authors:  Anna Bogdańska; Patryk Lipiński; Paulina Szymańska-Rożek; Aleksandra Jezela-Stanek; Dariusz Rokicki; Piotr Socha; Anna Tylki-Szymańska
Journal:  Orphanet J Rare Dis       Date:  2021-01-06       Impact factor: 4.123

5.  The development of end stage renal disease in two patients with PMM2-CDG.

Authors:  Henna Tiwary; Leah E Hecht; William J Brucker; Gerard T Berry; Nancy M Rodig
Journal:  JIMD Rep       Date:  2022-01-10

6.  PMM2-CDG and nephrotic syndrome: A case report.

Authors:  Giuseppe Banderali; Elisabetta Salvatici; Valentina Rovelli; Jaak Jaeken
Journal:  Clin Case Rep       Date:  2022-02-10

Review 7.  Diagnostic and Management Challenges in Congenital Nephrotic Syndrome.

Authors:  Ben Christopher Reynolds; Robert James Alan Oswald
Journal:  Pediatric Health Med Ther       Date:  2019-12-17
  7 in total

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