Literature DB >> 15840742

Congenital disorder of glycosylation id presenting with hyperinsulinemic hypoglycemia and islet cell hyperplasia.

Liangwu Sun1, Erik A Eklund, Wendy K Chung, Chao Wang, Jason Cohen, Hudson H Freeze.   

Abstract

CONTEXT: Inborn errors in protein glycosylation, such as the congenital disorders of glycosylation (CDGs), generate multifaceted syndromes that impair many organ systems. We here report the diagnosis of the third known patient with CDG-Id.
RESULTS: The patient's phenotype was extremely severe, and she succumbed at 19 d of age. Leading features included hyperinsulinemic hypoglycemia, and autopsy revealed islet cell hyperplasia with increased beta-cell mass. Other features were a Dandy-Walker malformation, facial dysmorphisms, and profound hypotonia. The patient carried a novel homozygous point mutation (512G>A) in the hALG3 gene, which encodes a mannosyltransferase. Lentiviral complementation with wild-type hALG3 corrects the biochemical defect in the patient's fibroblasts.
CONCLUSIONS: Our findings underscore the importance of proper glycosylation in several major organ systems and emphasize that CDG should be ruled out in patients with persistent hyperinsulinemic hypoglycemia of unknown etiology.

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Year:  2005        PMID: 15840742     DOI: 10.1210/jc.2005-0250

Source DB:  PubMed          Journal:  J Clin Endocrinol Metab        ISSN: 0021-972X            Impact factor:   5.958


  32 in total

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Review 3.  Liver involvement in congenital disorders of glycosylation (CDG). A systematic review of the literature.

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4.  A novel phenotype in N-glycosylation disorders: Gillessen-Kaesbach-Nishimura skeletal dysplasia due to pathogenic variants in ALG9.

Authors:  Emma Tham; Erik A Eklund; Anna Hammarsjö; Per Bengtson; Stefan Geiberger; Kristina Lagerstedt-Robinson; Helena Malmgren; Daniel Nilsson; Gintautas Grigelionis; Peter Conner; Peter Lindgren; Anna Lindstrand; Anna Wedell; Margareta Albåge; Katarzyna Zielinska; Ann Nordgren; Nikos Papadogiannakis; Gen Nishimura; Giedre Grigelioniene
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Review 5.  Cardiac complications of congenital disorders of glycosylation (CDG): a systematic review of the literature.

Authors:  D Marques-da-Silva; R Francisco; D Webster; V Dos Reis Ferreira; J Jaeken; T Pulinilkunnil
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6.  Identification of the gene encoding the alpha1,3-mannosyltransferase (ALG3) in Arabidopsis and characterization of downstream n-glycan processing.

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7.  Congenital disorder of glycosylation type Id (CDG Id): phenotypic, biochemical and molecular characterization of a new patient.

Authors:  A Rimella-Le-Huu; H Henry; I Kern; S Hanquinet; E Roulet-Perez; C J Newman; A Superti-Furga; L Bonafé; D Ballhausen
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8.  Glycan reductive isotope labeling for quantitative glycomics.

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Journal:  Anal Biochem       Date:  2009-02-10       Impact factor: 3.365

9.  Congenital disorder of glycosylation type Ia: heterogeneity in the clinical presentation from multivisceral failure to hyperinsulinaemic hypoglycaemia as leading symptoms in three infants with phosphomannomutase deficiency.

Authors:  B Shanti; M Silink; K Bhattacharya; N J Howard; K Carpenter; M Fietz; P Clayton; J Christodoulou
Journal:  J Inherit Metab Dis       Date:  2009-04-27       Impact factor: 4.982

10.  Comprehensive description of the phenotype of the first case of congenital disorder of glycosylation due to RFT1 deficiency (CDG In).

Authors:  P T Clayton; S Grunewald
Journal:  J Inherit Metab Dis       Date:  2009-03-11       Impact factor: 4.982

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