Andersen Syndrome
"Andersen Syndrome" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus,
MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure,
which enables searching at various levels of specificity.
A form of inherited long QT syndrome (or LQT7) that is characterized by a triad of potassium-sensitive periodic paralysis, VENTRICULAR ECTOPIC BEATS, and abnormal features such as short stature, low-set ears, and SCOLIOSIS. It results from mutations of KCNJ2 gene which encodes a channel protein (INWARD RECTIFIER POTASSIUM CHANNELS) that regulates resting membrane potential.
| Descriptor ID |
D050030
|
| MeSH Number(s) |
C14.280.067.565.070 C14.280.123.625.070 C16.131.240.400.715.070 C23.550.073.547.070
|
| Concept/Terms |
Andersen Syndrome- Andersen Syndrome
- Syndrome, Andersen
- Andersen Cardiodysrhythmic Periodic Paralysis
- Potassium-Sensitive Periodic Paralysis, Ventricular Ectopy, and Dysmorphic Features
- Andersen Tawil Syndrome
- Syndrome, Andersen Tawil
- Long QT Syndrome 7
- Periodic Paralysis, Potassium-Sensitive Cardiodysrhythmic Type
- Periodic Paralysis, Potassium Sensitive Cardiodysrhythmic Type
- Andersen-Tawil Syndrome
- Andersen Cardiodysrythmic Periodic Paralysis
|
Below are MeSH descriptors whose meaning is more general than "Andersen Syndrome".
Below are MeSH descriptors whose meaning is more specific than "Andersen Syndrome".
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Below are the most recent publications written about "Andersen Syndrome" by people in Profiles.