Literature DB >> 33407696

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

Anna Bogdańska1, Patryk Lipiński2, Paulina Szymańska-Rożek3, Aleksandra Jezela-Stanek4, Dariusz Rokicki2, Piotr Socha5, Anna Tylki-Szymańska6.   

Abstract

BACKGROUND: Congenital disorders of glycosylation (CDG) result from defects in the synthesis of glycans and the attachment of glycans to proteins and lipids. Our study aimed to describe the clinical, biochemical, and molecular findings of CDG patients, and to present the long-term follow-up.
MATERIAL AND METHODS: A single-center study (1995-2019 years) of patients with congenital disorders of N-glycosylation and combined N- and O-hypoglycosylation was performed.
RESULTS: Among 32 patients included into the study, there were 12 PMM2-CDG, 3 ALG13-CDG, 3 ALG1-CDG, 1 ALG3-CDG, 3 MPI-CDG, 1 PGM1-CDG, 4 SRD5A3-CDG, 1 DPAGT1-CDG, 3 ATP6AP1-CDG, 1 ATP6V0A2-CDG. The phenotypic and genotypic spectrum during long-term (in some cases over 20 years) observation was characterised and several measurements of serum Tf isoforms taken. Statistical analysis revealed strong negative correlation between asialo-Tf and tetrasialo-Tf, as well as between disialo-Tf and tetrasialo-Tf. Within CDG type I, no difference in % Tf isoforms was revealed between PMM2-CDG and non-PMM2-CDG patients. However, these two groups differed significantly in such diagnostic features as: cerebellar ataxia, failure to thrive, hypothyroidism, pericardial effusion, cardiomyopathy, inverted nipples, prolonged INR. The effect of treatment with mannose in 2 patients with MPI-CDG was assessed and we found that % of asialo-Tf, monosialo-Tf, and disialo-Tf was significantly lowered, whereas tetrasialo-Tf and pentasialo-Tf rose, coming closer or falling into the reference range.
CONCLUSIONS: The novel finding was an abnormal Tf IEF pattern in two ALG13-CDG patients and normal in one ALG1-CDG patient. Clinical manifestation of presented CDG patients was similar to that reported in the literature. Mannose supplementation in MPI-CDG patients, as well as galactose supplementation in PGM1-CDG patient, improved patients' clinical picture and Tf isoform profiles.

Entities:  

Keywords:  Congenital disorders of glycosylation; Follow-up; Glycosylation; Serum transferrin isoforms

Mesh:

Substances:

Year:  2021        PMID: 33407696      PMCID: PMC7789416          DOI: 10.1186/s13023-020-01657-5

Source DB:  PubMed          Journal:  Orphanet J Rare Dis        ISSN: 1750-1172            Impact factor:   4.123


  37 in total

1.  Nonimmune hydrops fetalis and congenital disorders of glycosylation: A systematic literature review.

Authors:  Mona M Makhamreh; Naiga Cottingham; Carlos R Ferreira; Seth Berger; Huda B Al-Kouatly
Journal:  J Inherit Metab Dis       Date:  2019-11-08       Impact factor: 4.982

2.  Carbohydrate deficient glycoprotein syndrome--like transferrin isoelectric focusing pattern in untreated fructosaemia.

Authors:  M Adamowicz; E Pronicka
Journal:  Eur J Pediatr       Date:  1996-04       Impact factor: 3.183

3.  Early-Onset Epileptic Encephalopathy in infants with different forms of Congenital Disorders of Glycosylation (CDG).

Authors:  Agata Fiumara; Rita Barone; Giuliana Del Campo; Pasquale Striano; Jaak Jaeken
Journal:  Brain Dev       Date:  2016-12-04       Impact factor: 1.961

Review 4.  Clinical, laboratory and molecular findings and long-term follow-up data in 96 French patients with PMM2-CDG (phosphomannomutase 2-congenital disorder of glycosylation) and review of the literature.

Authors:  Manuel Schiff; Céline Roda; Marie-Lorraine Monin; Alina Arion; Magali Barth; Nathalie Bednarek; Maud Bidet; Catherine Bloch; Nathalie Boddaert; Delphine Borgel; Anaïs Brassier; Alexis Brice; Arnaud Bruneel; Roger Buissonnière; Brigitte Chabrol; Marie-Chantal Chevalier; Valérie Cormier-Daire; Claire De Barace; Emmanuel De Maistre; Anne De Saint-Martin; Nathalie Dorison; Valérie Drouin-Garraud; Thierry Dupré; Bernard Echenne; Patrick Edery; François Feillet; Isabelle Fontan; Christine Francannet; François Labarthe; Cyril Gitiaux; Delphine Héron; Marie Hully; Sylvie Lamoureux; Dominique Martin-Coignard; Cyril Mignot; Gilles Morin; Tiffany Pascreau; Olivier Pincemaille; Michel Polak; Agathe Roubertie; Christel Thauvin-Robinet; Annick Toutain; Géraldine Viot; Sandrine Vuillaumier-Barrot; Nathalie Seta; Pascale De Lonlay
Journal:  J Med Genet       Date:  2017-09-27       Impact factor: 6.318

Review 5.  Renal involvement in PMM2-CDG, a mini-review.

Authors:  Ruqaiah Altassan; Peter Witters; Zubaida Saifudeen; Dulce Quelhas; Jaak Jaeken; Elena Levtchenko; David Cassiman; Eva Morava
Journal:  Mol Genet Metab       Date:  2017-11-28       Impact factor: 4.797

6.  Phenotypic and genotypic spectrum of congenital disorders of glycosylation type I and type II.

Authors:  Amal Al Teneiji; Theodora U J Bruun; Sarah Sidky; Dawn Cordeiro; Ronald D Cohn; Roberto Mendoza-Londono; Mahendranath Moharir; Julian Raiman; Komudi Siriwardena; Lianna Kyriakopoulou; Saadet Mercimek-Mahmutoglu
Journal:  Mol Genet Metab       Date:  2017-01-03       Impact factor: 4.797

7.  Multiple phenotypes in phosphoglucomutase 1 deficiency.

Authors:  Laura C Tegtmeyer; Stephan Rust; Monique van Scherpenzeel; Bobby G Ng; Marie-Estelle Losfeld; Sharita Timal; Kimiyo Raymond; Ping He; Mie Ichikawa; Joris Veltman; Karin Huijben; Yoon S Shin; Vandana Sharma; Maciej Adamowicz; Martin Lammens; Janine Reunert; Anika Witten; Esther Schrapers; Gert Matthijs; Jaak Jaeken; Daisy Rymen; Tanya Stojkovic; Pascal Laforêt; François Petit; Olivier Aumaître; Elzbieta Czarnowska; Monique Piraud; Teodor Podskarbi; Charles A Stanley; Reuben Matalon; Patricie Burda; Soraya Seyyedi; Volker Debus; Piotr Socha; Jolanta Sykut-Cegielska; Francjan van Spronsen; Linda de Meirleir; Pietro Vajro; Terry DeClue; Can Ficicioglu; Yoshinao Wada; Ron A Wevers; Dieter Vanderschaeghe; Nico Callewaert; Ralph Fingerhut; Emile van Schaftingen; Hudson H Freeze; Eva Morava; Dirk J Lefeber; Thorsten Marquardt
Journal:  N Engl J Med       Date:  2014-02-06       Impact factor: 91.245

8.  ALG12 mannosyltransferase defect in congenital disorder of glycosylation type lg.

Authors:  Claudia E Grubenmann; Christian G Frank; Susanne Kjaergaard; Eric G Berger; Markus Aebi; Thierry Hennet
Journal:  Hum Mol Genet       Date:  2002-09-15       Impact factor: 6.150

Review 9.  Congenital disorders of glycosylation with emphasis on cerebellar involvement.

Authors:  Rita Barone; Agata Fiumara; Jaak Jaeken
Journal:  Semin Neurol       Date:  2014-09-05       Impact factor: 3.420

10.  29 French adult patients with PMM2-congenital disorder of glycosylation: outcome of the classical pediatric phenotype and depiction of a late-onset phenotype.

Authors:  Marie-Lorraine Monin; Cyril Mignot; Pascale De Lonlay; Bénédicte Héron; Alice Masurel; Michèle Mathieu-Dramard; Catherine Lenaerts; Christel Thauvin; Marion Gérard; Emmanuel Roze; Aurélia Jacquette; Perrine Charles; Claire de Baracé; Valérie Drouin-Garraud; Philippe Khau Van Kien; Valérie Cormier-Daire; Michèle Mayer; Hélène Ogier; Alexis Brice; Nathalie Seta; Delphine Héron
Journal:  Orphanet J Rare Dis       Date:  2014-12-11       Impact factor: 4.123

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  5 in total

Review 1.  Nutrition interventions in congenital disorders of glycosylation.

Authors:  Suzanne W Boyer; Christin Johnsen; Eva Morava
Journal:  Trends Mol Med       Date:  2022-05-10       Impact factor: 15.272

2.  Neurological Consequences of Congenital Disorders of Glycosylation.

Authors:  Justyna Paprocka
Journal:  Adv Neurobiol       Date:  2023

3.  Congenital disorders of glycosylation: Prevalence, incidence and mutational spectrum in the Polish population.

Authors:  Patryk Lipiński; Anna Bogdańska; Anna Tylki-Szymańska
Journal:  Mol Genet Metab Rep       Date:  2021-02-11

4.  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

5.  Liver Involvement in Congenital Disorders of Glycosylation and Deglycosylation.

Authors:  Patryk Lipiński; Anna Bogdańska; Piotr Socha; Anna Tylki-Szymańska
Journal:  Front Pediatr       Date:  2021-07-05       Impact factor: 3.418

  5 in total

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