Aicardi-Goutieres syndrome in siblings

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

Aicardi-Goutieres syndrome in siblings

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

^*Corresponding author for this work

Research output: Contribution to journal › Article › peer-review

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 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

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title = "Aicardi-Goutieres syndrome in siblings",

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.",

author = "R. Koul and A. Chacko and S. Joshi and D. Sankhla",

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language = "English",

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AU - Koul, R.

AU - Chacko, A.

AU - Joshi, S.

AU - Sankhla, D.

PY - 2001

Y1 - 2001

N2 - 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.

AB - 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.

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