Warning: Undefined array key "mm" in /www/wwwroot/www.ai-bt.com/si.php on line 10 Deprecated: trim(): Passing null to parameter #1 ($string) of type string is deprecated in /www/wwwroot/www.ai-bt.com/si.php on line 10 Vanishing Weakness and Persistent Cardiac Dysrhythmia: Are We Dealing with Andersen Tawil Syndrome?

Literature DB >> 25616308

Vanishing Weakness and Persistent Cardiac Dysrhythmia: Are We Dealing with Andersen Tawil Syndrome?

P Jhansi Rani¹, P Yashodhara, N V Sundarachary, U Veeramma, Shaik Mansoor Elahi, Sridhar Amalakanti, A Lalitha.

Abstract

Andersen Tawil Syndrome (ATS) is a very rare type of periodic paralysis; the authors present a case report from South India with features that have not been reported earlier. This case suggests many unexplored hypotheses for the disease and argues the need for physician sensitization of this entity.

Entities: Disease

Mesh：

Substances：

Year: 2015 PMID： 25616308 DOI： 10.1007/s12098-014-1677-z

Source DB: PubMed Journal: Indian J Pediatr ISSN： 0019-5456 Impact factor: 1.967

Keyword Cloud
References

10 in total

1. ECG diagnosis: hypokalemia.

Authors: Joel T Levis
Journal: Perm J Date: 2012

2. Andersen syndrome: an association of periodic paralysis, cardiac arrhythmia and dysmorphic abnormalities.

Authors: Célia H Tengan; Antonio C Antunes; José R Bauab; José R Baubab; Gilmar F Prado; Gilberto M Manzano; Alberto A Gabbai
Journal: Arq Neuropsiquiatr Date: 2006-09 Impact factor: 1.420

3. Activation of inward rectifier K+ channels by hypoxia in rabbit coronary arterial smooth muscle cells.

Authors: Won Sun Park; Jin Han; Nari Kim; Jae-Hong Ko; Sung Joon Kim; Yung E Earm
Journal: Am J Physiol Heart Circ Physiol Date: 2005-12 Impact factor: 4.733

4. Andersen Tawil syndrome - periodic paralysis with dysmorphism.

Authors: Mahesh Kamate; Vivek Chetal
Journal: Indian Pediatr Date: 2011-01 Impact factor: 1.411

5. Electrocardiographic features in Andersen-Tawil syndrome patients with KCNJ2 mutations: characteristic T-U-wave patterns predict the KCNJ2 genotype.

Authors: Li Zhang; D Woodrow Benson; Martin Tristani-Firouzi; Louis J Ptacek; Rabi Tawil; Peter J Schwartz; Alfred L George; Minoru Horie; Gregor Andelfinger; Gregory L Snow; Ying-Hui Fu; Michael J Ackerman; G Michael Vincent
Journal: Circulation Date: 2005-05-23 Impact factor: 29.690

6. Functional and clinical characterization of KCNJ2 mutations associated with LQT7 (Andersen syndrome).

Authors: Martin Tristani-Firouzi; Judy L Jensen; Matthew R Donaldson; Valeria Sansone; Giovanni Meola; Angelika Hahn; Said Bendahhou; Hubert Kwiecinski; Anna Fidzianska; Nikki Plaster; Ying-Hui Fu; Louis J Ptacek; Rabi Tawil
Journal: J Clin Invest Date: 2002-08 Impact factor: 14.808

Vanishing Weakness and Persistent Cardiac Dysrhythmia: Are We Dealing with Andersen Tawil Syndrome?

1. ECG diagnosis: hypokalemia.

2. Andersen syndrome: an association of periodic paralysis, cardiac arrhythmia and dysmorphic abnormalities.

3. Activation of inward rectifier K+ channels by hypoxia in rabbit coronary arterial smooth muscle cells.

4. Andersen Tawil syndrome - periodic paralysis with dysmorphism.

5. Electrocardiographic features in Andersen-Tawil syndrome patients with KCNJ2 mutations: characteristic T-U-wave patterns predict the KCNJ2 genotype.

6. Functional and clinical characterization of KCNJ2 mutations associated with LQT7 (Andersen syndrome).

Review 7. Management and treatment of Andersen-Tawil syndrome (ATS).

8. Andersen-Tawil syndrome.

9. Brugada-like electrocardiographic patterns induced by hyperkalemia.

10. Defective potassium channel Kir2.1 trafficking underlies Andersen-Tawil syndrome.