Andersen-Tawil syndrome
Andersen-Tawil syndrome
Definition
Andersen's syndrome (AS) is 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.
Also known as Andersen cardiodysrhythmic periodic paralysis, Andersen syndrome, Andersen-Tawil syndrome, long QT syndrome 7, long QT syndrome type 7, LQT7 — per MONDO
Also identified as
- DOID 0050434 per MONDO
- ICD9 759.89 per MONDO
- MESH D050030 per MONDO
- NCIT C84559 per MONDO
- OMIM 170390 per MONDO
- Orphanet 37553 per MONDO
- SCTID 422348008 per MONDO
- UMLS C1563715 per MONDO
Affected Organs
| Organ | Involvement | Source |
|---|---|---|
| Cardiovascular system | Disease Has Associated Anatomic Site | NCIT · CC BY 4.0 |
| Cardiovascular system | Disease Has Primary Anatomic Site | NCIT · CC BY 4.0 |
| Heart | Disease Has Associated Anatomic Site | NCIT · CC BY 4.0 |
| Heart | Disease Has Primary Anatomic Site | NCIT · CC BY 4.0 |
| Respiratory system | Disease Has Associated Anatomic Site | NCIT · CC BY 4.0 |