Ellen D. Andersen
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 on July 10, 1939 in Copenhagen
- 1958-1966 Student of Nørre Gymnasium
- 1968 – Studied at the London School of Hygiene and Tropical Medicine
- 1969-1975 Training in internal medicine and cardiology at Rigshospitalet, and Bispebjerg hospital; Co-editor of “Symposium on Cardiac Arrhythmias” (1970)
- 1976-1982 Associate Professor of Internal Medicine, University Hospital of Copenhagen, Copenhagen, Denmark; Member of the board of the Danish Cardiological Society; Specialist in cardiology (1981)
- 1982-1993 chief physician at the Copenhagen General Practitioners’ Laboratory; General practitioner in Copenhagen
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. [OMIM #170390]
[aka *Andersen-Tawil syndrome (ATS); long QT syndrome 7; Andersen cardiodysrhythmic periodic paralysis]
1971 – Andersen et al reported the case of an 8-year-old boy with short of stature, hypertelorism, broad nasal root, mandibular hypoplasia, scaphocephaly, and clinodactyly V, as well as a defect of the soft and hard palate.
1994 – Tawil et al used the designation Andersen syndrome for the clinical triad of potassium-sensitive periodic paralysis, ventricular ectopy, and dysmorphic features. They found reports of 10 patients and added 4 new patients in 3 kindreds. All the patients had potassium-sensitive periodic paralysis without myotonia indistinguishable from other forms of hyperkalemic periodic paralysis. Tawil emphasized the variability of both the dysmorphic features and the cardiac manifestations.
- 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
- Biographical timeline: Flemming and Agnes Voss – Hørsholm, Denmark (Personal communication)
- 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.
- Andersen cardiodysrhythmic periodic paralysis. OMIM
the person behind the name
Graduated from Cardiff Medical School in 2017 with MBBCh and BSc in Psychology and Medicine. Currently working as a doctor in the emergency department at Sir Charles Gairdner Hospital in Perth, Australia.
Associate Professor Curtin Medical School, Curtin University. Emergency physician MA (Oxon) MBChB (Edin) FACEM FFSEM Sir Charles Gairdner Hospital. Passion for rugby; medical history; medical education; and asynchronous learning #FOAMed evangelist. Co-founder and CTO of Life in the Fast lane | Eponyms | Books | Twitter |