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Gitelman Syndrome in a School Boy Who Presented with Generalized Convulsion and Had a R642HR642W Mutation in the SLC12A3 Gene
المؤلفون المشاركون
Tanaka, Shin-ichiro
Makino, Shigeru
Awaguni, Hitoshi
Ikumi, Aki
Imashuku, Shinsaku
Shinozuka, Jun
Maruyama, Rikken
Tajima, Toshihiro
المصدر
العدد
المجلد 2014، العدد 2014 (31 ديسمبر/كانون الأول 2014)، ص ص. 1-5، 5ص.
الناشر
Hindawi Publishing Corporation
تاريخ النشر
2014-07-15
دولة النشر
مصر
عدد الصفحات
5
التخصصات الرئيسية
الملخص EN
An 8-year-old Japanese boy presented with a generalized convulsion.
He had hypokalemia (serum K 2.4 mEq/L), hypomagnesemia, and metabolic alkalosis (BE 5.7 mmol/L).
In addition, his plasma renin activity was elevated.
He was tentatively diagnosed with epilepsy on the basis of the electroencephalogram findings and was treated by potassium L-aspartate and carbamazepine to control the hypokalemia and seizure, respectively.
However, a year later, the patient continued to have similar abnormal laboratory data.
A presumptive diagnosis of Gitelman syndrome (GS) was then made and the patient’s peripheral blood mononuclear cells were subjected to sequence analysis of the SLC12A3 gene, which encodes a thiazide-sensitive sodium-chloride cotransporter.
The patient was found to have compound heterozygous mutations, namely, R642H inherited from his father and R642W inherited from his mother.
Thus, if a patient shows persistent hypokalemia and metabolic alkalosis, GS must be considered, even if the patient exhibits atypical clinical symptoms.
نمط استشهاد جمعية علماء النفس الأمريكية (APA)
Makino, Shigeru& Tajima, Toshihiro& Shinozuka, Jun& Ikumi, Aki& Awaguni, Hitoshi& Tanaka, Shin-ichiro…[et al.]. 2014. Gitelman Syndrome in a School Boy Who Presented with Generalized Convulsion and Had a R642HR642W Mutation in the SLC12A3 Gene. Case Reports in Pediatrics،Vol. 2014, no. 2014, pp.1-5.
https://search.emarefa.net/detail/BIM-459821
نمط استشهاد الجمعية الأمريكية للغات الحديثة (MLA)
Makino, Shigeru…[et al.]. Gitelman Syndrome in a School Boy Who Presented with Generalized Convulsion and Had a R642HR642W Mutation in the SLC12A3 Gene. Case Reports in Pediatrics No. 2014 (2014), pp.1-5.
https://search.emarefa.net/detail/BIM-459821
نمط استشهاد الجمعية الطبية الأمريكية (AMA)
Makino, Shigeru& Tajima, Toshihiro& Shinozuka, Jun& Ikumi, Aki& Awaguni, Hitoshi& Tanaka, Shin-ichiro…[et al.]. Gitelman Syndrome in a School Boy Who Presented with Generalized Convulsion and Had a R642HR642W Mutation in the SLC12A3 Gene. Case Reports in Pediatrics. 2014. Vol. 2014, no. 2014, pp.1-5.
https://search.emarefa.net/detail/BIM-459821
نوع البيانات
مقالات
لغة النص
الإنجليزية
الملاحظات
Includes bibliographical references
رقم السجل
BIM-459821
قاعدة معامل التأثير والاستشهادات المرجعية العربي "ارسيف Arcif"
أضخم قاعدة بيانات عربية للاستشهادات المرجعية للمجلات العلمية المحكمة الصادرة في العالم العربي
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