Literature DB >> 19176971

Prenatal cardiac ultrasound finding in congenital disorder of glycosylation type 1a.

A Malhotra1, A Pateman, R Chalmers, D Coman, S Menahem.   

Abstract

We present the antenatal cardiac findings in an infant in whom a postnatal diagnosis of congenital disorder of glycosylation type Ia (CDG-Ia) was confirmed. The antenatal findings at 34 weeks' gestation included biventricular cardiac hypertrophy with pericardial effusion, multiple skeletal anomalies and cerebral ventricular dilatation. A severe CDG-Ia multisystem clinical phenotype evolved in the postnatal period, with the infant succumbing at 3.5 weeks of age secondary to a large pericardial effusion with tamponade. A literature review suggests that this is the first case of cardiac manifestations of CDG-Ia observed antenatally. We would also like to suggest that CDG-Ia should be considered and if possible prenatal diagnosis performed in cases with hypertrophic cardiomyopathy, and/or pericardial effusion. (c) 2009 S. Karger AG, Basel.

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Year:  2009        PMID: 19176971     DOI: 10.1159/000196816

Source DB:  PubMed          Journal:  Fetal Diagn Ther        ISSN: 1015-3837            Impact factor:   2.587


  8 in total

Review 1.  Recognizable phenotypes in CDG.

Authors:  Carlos R Ferreira; Ruqaia Altassan; Dorinda Marques-Da-Silva; Rita Francisco; Jaak Jaeken; Eva Morava
Journal:  J Inherit Metab Dis       Date:  2018-04-13       Impact factor: 4.982

2.  Hypoglycemia in CDG patients due to PMM2 mutations: Follow up on hyperinsulinemic patients.

Authors:  Hossein Moravej; Ruqaiah Altassan; Jaak Jaeken; Gregory M Enns; Carolyn Ellaway; Shanti Balasubramaniam; Pascale De Lonlay; David Coman; Saadet Mercimek-Andrews; Peter Witters; Eva Morava
Journal:  JIMD Rep       Date:  2019-11-25

Review 3.  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
Journal:  J Inherit Metab Dis       Date:  2017-07-19       Impact factor: 4.982

4.  A novel mutation and first report of dilated cardiomyopathy in ALG6-CDG (CDG-Ic): a case report.

Authors:  Mohammed Al-Owain; Sarar Mohamed; Namik Kaya; Ahmad Zagal; Gert Matthijs; Jaak Jaeken
Journal:  Orphanet J Rare Dis       Date:  2010-04-16       Impact factor: 4.123

Review 5.  Cardiomyopathy in the congenital disorders of glycosylation (CDG): a case of late presentation and literature review.

Authors:  E J Footitt; A Karimova; M Burch; T Yayeh; T Dupré; S Vuillaumier-Barrot; I Chantret; S E H Moore; N Seta; S Grunewald
Journal:  J Inherit Metab Dis       Date:  2009-09-07       Impact factor: 4.982

6.  From discrete dilated cardiomyopathy to successful cardiac transplantation in congenital disorders of glycosylation due to dolichol kinase deficiency (DK1-CDG).

Authors:  Livia Kapusta; Nili Zucker; George Frenckel; Benjamin Medalion; Tuvia Ben Gal; Einat Birk; Hanna Mandel; Nadim Nasser; Sarah Morgenstern; Andreas Zuckermann; Dirk J Lefeber; Arjen de Brouwer; Ron A Wevers; Avraham Lorber; Eva Morava
Journal:  Heart Fail Rev       Date:  2013-03       Impact factor: 4.214

7.  A 6-Month-Old Infant with Severe Failure to Thrive during COVID-19 Pandemic.

Authors:  Xinying Hong; Hana Alharbi; Daniah Albokhari; Andrew C Edmondson; Miao He
Journal:  Clin Chem       Date:  2022-07-03       Impact factor: 12.167

8.  Hyperinsulinism May Be Underreported in Hypoglycemic Patients with Phosphomannomutase 2 Deficiency

Authors:  Doğuş Vurallı; Yılmaz Yıldız; Alev Ozon; Ali Dursun; Nazlı Gönç; Ayşegül Tokatlı; H Serap Sivri; Ayfer Alikaşifoğlu
Journal:  J Clin Res Pediatr Endocrinol       Date:  2022-03-21
  8 in total

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