ANDERSENS-SYNDROME - POTASSIUM-SENSITIVE PERIODIC PARALYSIS, VENTRICULAR ECTOPY, AND DYSMORPHIC FEATURES

被引：244

作者：

TAWIL, R

PTACEK, LJ

PAVLAKIS, SG

DEVIVO, DC

PENN, AS

OZDEMIR, C

GRIGGS, RC

机构：

[1] DEPT NEUROL,GORELL MOLEC BIOL LAB,ROCHESTER,NY

[2] UNIV UTAH,SCH MED,DEPT HUMAN GENET,DEPT NEUROL,SALT LAKE CITY,UT 84132

[3] NEW YORK HOSP,CORNELL MED CTR,DIV PEDIAT NEUROL,NEW YORK,NY 10021

[4] COLUMBIA UNIV,COLL PHYSICIANS & SURGEONS,DEPT NEUROL,NEW YORK,NY 10032

[5] COLUMBIA UNIV,COLL PHYSICIANS & SURGEONS,DEPT NEUROL & PEDIAT,NEW YORK,NY

[6] UNIV ISTANBUL,ISTANBUL FAC MED,DEPT NEUROL,ISTANBUL,TURKEY

来源：

ANNALS OF NEUROLOGY | 1994年 / 35卷 / 03期

关键词：

D O I：

10.1002/ana.410350313

中图分类号：

R74 [神经病学与精神病学];

学科分类号：

摘要：

Andersen's syndrome is a clinically distinct form of potassium-sensitive periodic paralysis associated with cardiac dysrhythmias. The subtle nature of the cardiac and dysmorphic features may delay the recognition of this syndrome and its potentially lethal cardiac dysrhythmias. The genetic defect in Andersen's syndrome is not genetically linked to other forms of potassium-sensitive periodic paralysis and is probably distinct from the long QT syndrome locus.

引用

页码：326 / 330

页数：5

共 23 条

[1] INTERMITTENT MUSCULAR WEAKNESS, EXTRASYSTOLES, AND MULTIPLE DEVELOPMENTAL ANOMALIES - NEW SYNDROME [J].