Andersen-Tawil Syndrome – Periodic Paralysis with Dysmorphism.
Indian Pediatr
;
2011 Jan; 48(1): 64-65
Artigo
em Inglês
| 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.
Texto completo:
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Índice:
IMSEAR (Sudeste Asiático)
Idioma:
Inglês
Revista:
Indian Pediatr
Ano de publicação:
2011
Tipo de documento:
Artigo
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