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 |
|---|---|
| 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