Ellen Damgaard Andersen (1939 – ) Danish physician.
In 1971, Andersen and her colleagues (Peter Krasilnikoff and Hans Overad) published the case of an 8-year-old child who suffered episodes of paralysis, extrasystoles and characteristic developmental abnormalities (low set ears, hypertelorism, mandibular hypoplasia, broad root of nose, clinodactyly). The disorder known as Andersen syndrome or Andersen-Tawil syndrome.
- Born 10 July 1939
Andersen Syndrome (1971)
Autosomal dominant trait with clinical manifestations including potassium sensitive periodic paralysis, prolongation of the QT interval, ventricular arrhythmias, and characteristic physical features including low-set ears, micrognathia, and clinodactyly. Andersen et al reported the case of a 8-years old with short stature, hypertelorism, broad nasal root, and defect of soft and hard palate.
[Andersen-Tawil syndrome (ATS); long QT syndrome 7]
- Andersen ED, Krasilnikoff PA, Overvad H. Intermittent muscular weakness, extrasystoles and multiple developmental anomalies. A new syndrome? Acta Paediatr Scand. 1971; 60: 559–564.
- Pietersen AH, Andersen ED, Sandøe E. Atrial fibrillation in the Wolff-Parkinson-White syndrome. Am J Cardiol. 1992;70(5):38A-43A
- Gulløv AL, Koefoed BG, Petersen P, et al. Fixed minidose warfarin and aspirin alone and in combination vs adjusted-dose warfarin for stroke prevention in atrial fibrillation: Second Copenhagen Atrial Fibrillation, Aspirin, and Anticoagulation Study. Arch Intern Med. 1998;158(14):1513-1521.
- Thomas E, Aziz-Donnelly A, Garcia-Santibanez R. Women in the History of Neuromuscular Medicine. Neuromuscular Disorders. 2019; 29: 698-703
- Tawil R, Ptacek LJ, Pavlakis SG, et al. Andersen’s syndrome: potassium-sensitive periodic paralysis, ventricular ectopy, and dysmorphic features. Ann Neurol. 1994;35(3):326-330.
- Veerapandiyan A, Statland JM, Tawil R. Andersen-Tawil Syndrome. In: Adam MP, Ardinger HH, Pagon RA, et al., eds. GeneReviews®. Seattle (WA): University of Washington, Seattle; November 22, 2004.
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