Case ReportCase Report
Open Access
Hypokalemic periodic paralysis due to CACNA1S gene mutation
Khalid A. Alhasan, Mohammed S. Abdallah, Jameela A. Kari and Fahad A. Bashiri
Neurosciences Journal July 2019, 24 (3) 225-230; DOI: https://doi.org/10.17712/nsj.2018.3.20180005
Khalid A. Alhasan
From the Division of Pediatric Nephrology (Alhasan, Abdallah, Bashiri), Pediatric Department, College of Medicine, King Khalid University Hospital, King Saud University, Riyadh, and from Pediatric Nephrology Center of Excellence and Division of Pediatric Nephrology (Kari), Department of Pediatrics, King Abdulaziz University, Jeddah, Kingdom of Saudi Arabia
MDMohammed S. Abdallah
From the Division of Pediatric Nephrology (Alhasan, Abdallah, Bashiri), Pediatric Department, College of Medicine, King Khalid University Hospital, King Saud University, Riyadh, and from Pediatric Nephrology Center of Excellence and Division of Pediatric Nephrology (Kari), Department of Pediatrics, King Abdulaziz University, Jeddah, Kingdom of Saudi Arabia
MRCPCHJameela A. Kari
From the Division of Pediatric Nephrology (Alhasan, Abdallah, Bashiri), Pediatric Department, College of Medicine, King Khalid University Hospital, King Saud University, Riyadh, and from Pediatric Nephrology Center of Excellence and Division of Pediatric Nephrology (Kari), Department of Pediatrics, King Abdulaziz University, Jeddah, Kingdom of Saudi Arabia
FRCPCHFahad A. Bashiri
From the Division of Pediatric Nephrology (Alhasan, Abdallah, Bashiri), Pediatric Department, College of Medicine, King Khalid University Hospital, King Saud University, Riyadh, and from Pediatric Nephrology Center of Excellence and Division of Pediatric Nephrology (Kari), Department of Pediatrics, King Abdulaziz University, Jeddah, Kingdom of Saudi Arabia
MDReferences
- ↵
- Statland JM,
- Barohn RJ
- ↵
- Adam MP,
- Ardinger HH,
- Pagon RA,
- Wallace SE,
- Bean LJ,
- Stephens K
- Vicart S,
- Sternberg D,
- Arzel-Hézode M,
- Franques J,
- Bendahhou S,
- Lory P,
- et al.
- ↵
- Al Moteri BL,
- Aslam M
- ↵
- Aldasouqi S,
- Bokhari SA,
- Khan PM,
- Al-Zahrani AS
- ↵
- Statland JM,
- Fontaine B,
- Hanna MG,
- Johnson NE,
- Kissel JT,
- Sansone VA,
- et al.
- ↵
- Matthews E,
- Portaro S,
- Ke Q,
- Sud R,
- Haworth A,
- Davis MB,
- et al.
- ↵
- Fontaine B
- ↵
- Männikkö R,
- Kullmann DM
- ↵
- Ke T,
- Gomez CR,
- Mateus HE,
- Castano JA,
- Wang QK
- ↵
- Wang XY,
- Ren BW,
- Yong ZH,
- Xu HY,
- Fu QX,
- Yao HB
- ↵
- Sternberg D,
- Maisonobe T,
- Jurkat-Rott K,
- Nicole S,
- Launay E,
- Chauveau D,
- et al.
- ↵
- Matthews E,
- Labrum R,
- Sweeney MG,
- Sud R,
- Haworth A,
- Chinnery PF,
- et al.
- ↵
- Cavel-Greant D,
- Lehmann-Horn F,
- Jurkat-Rott K
In this issue
Hypokalemic periodic paralysis due to CACNA1S gene mutation
Khalid A. Alhasan, Mohammed S. Abdallah, Jameela A. Kari, Fahad A. Bashiri
Neurosciences Journal Jul 2019, 24 (3) 225-230; DOI: 10.17712/nsj.2018.3.20180005
Jump to section
Related Articles
- No related articles found.
Cited By...
- No citing articles found.