Literature DB >> 22374380

Hypertrophic cardiomyopathy with cardiac rupture and tamponade caused by congenital disorder of glycosylation type Ia.

Laura I Rudaks1, Chad Andersen, T Y Khong, Andrew Kelly, Michael Fietz, Christopher P Barnett.   

Abstract

Hypertrophic cardiomyopathy (HCM) is a rare presenting feature of congenital disorder of glycosylation type Ia (CDG-Ia). We report two female siblings with CDG-Ia and cardiomyopathy. Patient no. 1 died at 12 days of age from cardiac rupture and tamponade, which has not previously been reported in CDG-Ia. The second patient died at 2 months of age from HCM. The severe cardiac manifestations seen in our patients emphasize the importance of early cardiac assessment in all patients with CDG-Ia.

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Year:  2012        PMID: 22374380     DOI: 10.1007/s00246-012-0214-y

Source DB:  PubMed          Journal:  Pediatr Cardiol        ISSN: 0172-0643            Impact factor:   1.655


  7 in total

1.  Congenital disorder of glycosylation type Ia: a clinicopathological report of a newborn infant with cerebellar pathology.

Authors:  E Aronica; A A M W van Kempen; M van der Heide; B T Poll-The; H J van Slooten; D Troost; J M Rozemuller-Kwakkel
Journal:  Acta Neuropathol       Date:  2005-02-16       Impact factor: 17.088

2.  Genotypes and phenotypes of patients in the UK with carbohydrate-deficient glycoprotein syndrome type 1.

Authors:  F Imtiaz; V Worthington; M Champion; C Beesley; J Charlwood; P Clayton; G Keir; N Mian; B Winchester
Journal:  J Inherit Metab Dis       Date:  2000-03       Impact factor: 4.982

Review 3.  Carbohydrate-deficient glycoprotein syndrome type IA (phosphomannomutase-deficiency).

Authors:  H Carchon; E Van Schaftingen; G Matthijs; J Jaeken
Journal:  Biochim Biophys Acta       Date:  1999-10-08

Review 4.  Congenital disorders of glycosylation.

Authors:  Jaak Jaeken
Journal:  Ann N Y Acad Sci       Date:  2010-12       Impact factor: 5.691

5.  Severe transient myocardial ischaemia caused by hypertrophic cardiomyopathy in a patient with congenital disorder of glycosylation type Ia.

Authors:  Thorsten Marquardt; Georg Hülskamp; Josef Gehrmann; Volker Debus; Erik Harms; Hans Gerd Kehl
Journal:  Eur J Pediatr       Date:  2002-08-22       Impact factor: 3.183

Review 6.  Hypertrophic cardiomyopathy.

Authors:  Jeffrey A Towbin
Journal:  Pacing Clin Electrophysiol       Date:  2009-07       Impact factor: 1.976

Review 7.  Cardiomyopathy in congenital disorders of glycosylation.

Authors:  Josef Gehrmann; Kristina Sohlbach; Michael Linnebank; Hans-Josef Böhles; Stephan Buderus; Hans Gerd Kehl; Johannes Vogt; Erik Harms; Thorsten Marquardt
Journal:  Cardiol Young       Date:  2003-08       Impact factor: 1.093

  7 in total
  7 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

Review 2.  Infant with cardiomyopathy: When to suspect inborn errors of metabolism?

Authors:  Stephanie L Byers; Can Ficicioglu
Journal:  World J Cardiol       Date:  2014-11-26

3.  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

4.  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 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
Journal:  J Inherit Metab Dis       Date:  2017-07-19       Impact factor: 4.982

6.  A case of congenital disorder of glycosylation ia presented with recurrent pericardial effusion.

Authors:  Sedat Işıkay; Osman Başpınar; Kutluhan Yılmaz
Journal:  Iran J Pediatr       Date:  2014-07-19       Impact factor: 0.364

7.  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
  7 in total

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