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Синдром Андерсена-Тавіла

ORPHA:37553· ICD-10 G72.3· Andersen-Tawil syndrome

Визначення(English summary)

A rare disorder characterized by periodic muscle paralysis, prolongation of the QT interval with a variety of ventricular arrhythmias (leading to predisposition to sudden cardiac death) and characteristic physical features: short stature, scoliosis, low-set ears, hypertelorism, broad nasal root, micrognathia, clinodactyly, brachydactyly and syndactyly.

Поширеність
Unknown
Успадкування
Autosomal dominant
Вік початку
Childhood