Andersen Tawil syndrome - periodic paralysis with dysmorphism.

Abstract:

:Andersen Tawil syndrome is a rare type of channelopathy characterized by the presence of periodic paralysis, cardiac arrhythmia (prolonged QT interval or ventricular arrhythmia) and distinct dysmorphic abnormalities. It is a type of potassium channelopathy that occurs sporadically or by autosomal dominant inheritance. We report a 14 year old boy with Andersen-Tawil syndrome.

journal_name

Indian Pediatr

journal_title

Indian pediatrics

authors

Kamate M,Chetal V

doi

10.1007/s13312-011-0008-y

subject

Has Abstract

pub_date

2011-01-01 00:00:00

pages

64-5

issue

1

eissn

0019-6061

issn

0974-7559

journal_volume

48

pub_type

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