Aicardi-Goutieres syndrome in siblings

R. Koul, A. Chacko, S. Joshi, D. Sankhla

Research output: Contribution to journalArticle

4 Citations (Scopus)

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 languageEnglish
Pages (from-to)759-761
Number of pages3
JournalJournal of Child Neurology
Volume16
Issue number10
Publication statusPublished - 2001

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Siblings
Arab World
Lymphocytosis
Cerebrospinal Fluid
Infection
Aicardi-Goutieres syndrome

ASJC Scopus subject areas

  • Clinical Neurology
  • Pediatrics, Perinatology, and Child Health

Cite this

Aicardi-Goutieres syndrome in siblings. / Koul, R.; Chacko, A.; Joshi, S.; Sankhla, D.

In: Journal of Child Neurology, Vol. 16, No. 10, 2001, p. 759-761.

Research output: Contribution to journalArticle

Koul, R, Chacko, A, Joshi, S & Sankhla, D 2001, 'Aicardi-Goutieres syndrome in siblings', Journal of Child Neurology, vol. 16, no. 10, pp. 759-761.
Koul, R. ; Chacko, A. ; Joshi, S. ; Sankhla, D. / Aicardi-Goutieres syndrome in siblings. In: Journal of Child Neurology. 2001 ; Vol. 16, No. 10. pp. 759-761.
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