Literature DB >> 24932094

Transient complete atrioventricular block in a preterm neonate with congenital myotonic dystrophy: case report.

Hee Na Kim1, Young Kuk Cho1, Joo Hyun Cho1, Eun Mi Yang1, Eun Song Song1, Young Youn Choi1.   

Abstract

Congenital myotonic dystrophy (CMD) is an inherited neuromuscular disorder with cardiac rhythm abnormalities that may occur as a child grows. No report has described complete atrioventricular (AV) block detected in a neonate with CMD. We report a floppy infant of 31(+4) weeks gestation with complete AV block at birth, who was diagnosed with CMD by Southern analysis. She recovered from complete AV block 32 hr after temporary transcutaneous pacing was applied. To the best our knowledge, this is the first recorded case of a complete AV block accompanied by CMD during the neonatal period. When a newborn has a complete AV block, the physician should consider the possibility of the CMD and conduct a careful physical examination.

Entities:  

Keywords:  Complete Atrioventricular Block; Congenital Myotonic Dystrophy; Pacing

Mesh:

Substances:

Year:  2014        PMID: 24932094      PMCID: PMC4055826          DOI: 10.3346/jkms.2014.29.6.879

Source DB:  PubMed          Journal:  J Korean Med Sci        ISSN: 1011-8934            Impact factor:   2.153


  15 in total

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Journal:  Heart       Date:  2002-12       Impact factor: 5.994

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Review 5.  Congenital complete heart block: an international study of the natural history.

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Review 6.  Cardiac manifestations of myotonic dystrophy type 1.

Authors:  Helle Petri; John Vissing; Nanna Witting; Henning Bundgaard; Lars Køber
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7.  Different patterns of obstetric complications in myotonic dystrophy in relation to the disease status of the fetus.

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Journal:  Am J Med Genet       Date:  1998-12-04

8.  Detection of an unstable fragment of DNA specific to individuals with myotonic dystrophy.

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Journal:  Nature       Date:  1992-02-06       Impact factor: 49.962

9.  Congenital myotonic dystrophy: assisted ventilation duration and outcome.

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Journal:  Pediatrics       Date:  2004-04       Impact factor: 7.124

10.  Molecular basis of myotonic dystrophy: expansion of a trinucleotide (CTG) repeat at the 3' end of a transcript encoding a protein kinase family member.

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  2 in total

Review 1.  Heart Disease in Disorders of Muscle, Neuromuscular Transmission, and the Nerves.

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Journal:  Korean Circ J       Date:  2016-03-21       Impact factor: 3.243

2.  Intergenerational Influence of Gender and the DM1 Phenotype of the Transmitting Parent in Korean Myotonic Dystrophy Type 1.

Authors:  Ji Yoon Han; Woori Jang; Joonhong Park
Journal:  Genes (Basel)       Date:  2022-08-17       Impact factor: 4.141

  2 in total

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