ملخص
Two siblings with familial encephalopathy, calcification of the basal ganglia, and cerebrospinal fluid lymphocytosis, constituting the triad of Aicardi-Goutieres syndrome, are reported. This syndrome resembles congenital intrauterine infections, which must be meticulously excluded. Aicardi-Goutieres syndrome is extremely rare and is being reported from the Arab world for the first time to our knowledge.
اللغة الأصلية | English |
---|---|
الصفحات (من إلى) | 759-761 |
عدد الصفحات | 3 |
دورية | Journal of Child Neurology |
مستوى الصوت | 16 |
رقم الإصدار | 10 |
المعرِّفات الرقمية للأشياء | |
حالة النشر | Published - 2001 |
ASJC Scopus subject areas
- ???subjectarea.asjc.2700.2735???
- ???subjectarea.asjc.2700.2728???