Andersen-Tawil Syndrome – Periodic Paralysis with Dysmorphism.
Indian Pediatr
;
2011 Jan; 48(1): 64-65
Article
in English
| IMSEAR
| ID: sea-168750
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.
Full text:
Available
Index:
IMSEAR (South-East Asia)
Language:
English
Journal:
Indian Pediatr
Year:
2011
Type:
Article
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