phenytoin has been researched along with Andersen Syndrome in 1 studies
Andersen Syndrome: 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.
Excerpt | Relevance | Reference |
---|---|---|
"Phenytoin was considered for control of symptomatic VA in three patients." | 1.51 | Short-term response to phenytoin sodium in Andersen-Tawil syndrome-1 with a cardiac-dominant phenotype. ( Augustine, AJ; Bhavani, GS; Girisha, KM; Kamath, P; Kedambadi, RC; Pai, R; Pasha, SW; Prabhu, MA; Rai, MK, 2019) |
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 0 (0.00) | 18.2507 |
2000's | 0 (0.00) | 29.6817 |
2010's | 1 (100.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Rai, MK | 1 |
Pai, R | 1 |
Prabhu, MA | 1 |
Pasha, SW | 1 |
Kedambadi, RC | 1 |
Kamath, P | 1 |
Augustine, AJ | 1 |
Bhavani, GS | 1 |
Girisha, KM | 1 |
1 other study available for phenytoin and Andersen Syndrome
Article | Year |
---|---|
Short-term response to phenytoin sodium in Andersen-Tawil syndrome-1 with a cardiac-dominant phenotype.
Topics: Adolescent; Adult; Algorithms; Andersen Syndrome; Arrhythmias, Cardiac; Female; Humans; Male; Pedigr | 2019 |