Literature DB >> 24861851

Andersen-Tawil syndrome: report of 3 novel mutations and high risk of symptomatic cardiac involvement.

Anna Kostera-Pruszczyk1, Anna Potulska-Chromik, Piotr Pruszczyk, Katarzyna Bieganowska, Maria Miszczak-Knecht, Piotr Bienias, Krzysztof Szczałuba, Hsien-Yang Lee, Emily Quinn, Rafal Ploski, Anna Kaminska, Louis J Ptáček.   

Abstract

INTRODUCTION: Andersen-Tawil syndrome (ATS) is a potassium channelopathy affecting cardiac and skeletal muscle. Periodic paralysis is a presenting symptom in some patients, whereas, in others, symptomatic arrhythmias or prolongation of QT in echocardiographic recordings will lead to diagnosis of ATS. Striking intrafamilial variability of expression of KCNJ2 mutations and rarity of the syndrome may lead to misdiagnosis.
METHODS: We report 15 patients from 8 Polish families with ATS, including 3 with novel KCNJ2 mutations.
RESULTS: All patients had dysmorphic features; periodic paralysis affected males more frequently than females (80% vs. 20%), and most attacks were normokalemic. Two patients (with T75M and T309I mutations) had aborted sudden cardiac death. An implantable cardioverter-defibrillator was utilized in 40% of cases.
CONCLUSIONS: KCNJ2 mutations cause a variable phenotype, with dysmorphic features seen in all patients studied, a high penetrance of periodic paralysis in males and ventricular arrhythmia with a risk of sudden cardiac death.
© 2014 Wiley Periodicals, Inc.

Entities:  

Keywords:  KCNJ2; channelopathy; long QT; periodic paralysis; ventricular arrhythmia

Mesh:

Substances:

Year:  2014        PMID: 24861851     DOI: 10.1002/mus.24293

Source DB:  PubMed          Journal:  Muscle Nerve        ISSN: 0148-639X            Impact factor:   3.217


  5 in total

1.  Andersen-Tawil syndrome: Clinical presentation and predictors of symptomatic arrhythmias - Possible role of polymorphisms K897T in KCNH2 and H558R in SCN5A gene.

Authors:  Michalina Krych; Elżbieta Katarzyna Biernacka; Joanna Ponińska; Piotr Kukla; Artur Filipecki; Robert Gajda; Can Hasdemir; Charles Antzelevitch; Agnieszka Kosiec; Małgorzata Szperl; Rafał Płoski; Maria Trusz-Gluza; Katarzyna Mizia-Stec; Piotr Hoffman
Journal:  J Cardiol       Date:  2017-03-21       Impact factor: 3.159

Review 2.  Inward rectifier potassium (Kir) channels in the retina: living our vision.

Authors:  Katie M Beverley; Bikash R Pattnaik
Journal:  Am J Physiol Cell Physiol       Date:  2022-08-01       Impact factor: 5.282

3.  Andersen-Tawil Syndrome With Novel Mutation in KCNJ2: Case Report.

Authors:  Jisook Yim; Kyoung Bo Kim; Minsun Kim; Gun Dong Lee; Myungshin Kim
Journal:  Front Pediatr       Date:  2022-01-31       Impact factor: 3.418

4.  Propafenone is not effective for severe ventricular arrhythmias in Andersen-Tawil syndrome.

Authors:  Piotr Bienias; Anna Kostera-Pruszczyk; Maria Miszczak-Knecht; Michał Ciurzyński; Piotr Pruszczyk
Journal:  Arch Med Sci       Date:  2016-06-30       Impact factor: 3.318

5.  Phenotypic variability in a series of four pediatric patients with Andersen-Tawil syndrome: A Saudi experience.

Authors:  Norah A Alrashed; Waleed M Al-Manea; Sahar A Tulbah; Zuhair N Al-Hassnan
Journal:  Int J Pediatr Adolesc Med       Date:  2019-06-14
  5 in total

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