Literature DB >> 27145478

Clinical features and long exercise test in Chinese patients with Andersen-Tawil syndrome.

Jie Song1, Sushan Luo1, Xin Cheng1, Dongyue Yue1, Wenhua Zhu1, Jie Lin1, Jun Huang2, Jiahong Lu1, Chongbo Zhao1, Kai Qiao2.   

Abstract

INTRODUCTION: Andersen-Tawil syndrome (ATS) is a rare multisystem channelopathy characterized by periodic paralysis, ventricular arrhythmias, and developmental dysmorphology. There are few reports concerning ATS in the Chinese population. We analyzed clinical features and evaluated the long exercise test as a tool for diagnosis of periodic paralysis in ATS.
METHODS: Direct sequencing of KCNJ2 was performed in 12 subjects from mainland China with suspected ATS. Clinical features, therapeutic responses, and long exercise tests (LET) were retrospectively analyzed.
RESULTS: Twelve patients were genetically confirmed to have ATS. A small mandible and clinodactyly were demonstrated in all patients. Premature ventricular contractions were the most prevalent form of cardiac arrhythmia. The LET revealed an early amplitude decrement.
CONCLUSIONS: Chinese ATS patients shared some common clinical features with reported subjects in other countries. An early amplitude decrement in LET may be useful for diagnosis of ATS. Muscle Nerve 54: 1059-1063, 2016.
© 2016 Wiley Periodicals, Inc.

Entities:  

Keywords:  Andersen-Tawil syndrome; KCNJ2; amplitude decrement; long exercise test; methazolamide; periodic paralysis

Mesh:

Substances:

Year:  2016        PMID: 27145478     DOI: 10.1002/mus.25169

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


  5 in total

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Journal:  Am J Physiol Cell Physiol       Date:  2022-08-01       Impact factor: 5.282

2.  Identification of gene mutations in patients with primary periodic paralysis using targeted next-generation sequencing.

Authors:  Sushan Luo; Minjie Xu; Jian Sun; Kai Qiao; Jie Song; Shuang Cai; Wenhua Zhu; Lei Zhou; Jianying Xi; Jiahong Lu; Xiaohua Ni; Tonghai Dou; Chongbo Zhao
Journal:  BMC Neurol       Date:  2019-05-08       Impact factor: 2.474

Review 3.  CAMPTODACTYLY AND CLINODACTYLY - NEW UNDERSTANDING OF KNOWN DEFORMITIES.

Authors:  Matija Matošević; Lovro Lamot; Darko Antičević
Journal:  Acta Clin Croat       Date:  2022-02       Impact factor: 0.780

4.  Characterization of Loss-Of-Function KCNJ2 Mutations in Atypical Andersen Tawil Syndrome.

Authors:  Pauline Le Tanno; Mathilde Folacci; Jean Revilloud; Laurence Faivre; Gabriel Laurent; Lucile Pinson; Pascal Amedro; Gilles Millat; Alexandre Janin; Michel Vivaudou; Nathalie Roux-Buisson; Julien Fauré
Journal:  Front Genet       Date:  2021-11-25       Impact factor: 4.599

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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