Abstract
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.
Original language | English |
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Pages (from-to) | 759-761 |
Number of pages | 3 |
Journal | Journal of Child Neurology |
Volume | 16 |
Issue number | 10 |
Publication status | Published - 2001 |
ASJC Scopus subject areas
- Clinical Neurology
- Pediatrics, Perinatology, and Child Health