Aicardi-Goutieres syndrome in siblings

Roshan Koul; Alexander Chacko; Surendranath Joshi; Dilip Sankhla

doi:10.1177/088307380101601009

Aicardi-Goutieres syndrome in siblings

Roshan Koul^*, Alexander Chacko, Surendranath Joshi, Dilip 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
DOIs	https://doi.org/10.1177/088307380101601009
Publication status	Published - 2001
Externally published	Yes

ASJC Scopus subject areas

Pediatrics, Perinatology, and Child Health
Clinical Neurology

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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 = "Roshan Koul and Alexander Chacko and Surendranath Joshi and Dilip Sankhla",

year = "2001",

doi = "10.1177/088307380101601009",

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AU - Koul, Roshan

AU - Chacko, Alexander

AU - Joshi, Surendranath

AU - Sankhla, Dilip

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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ER -

Aicardi-Goutieres syndrome in siblings

Abstract

ASJC Scopus subject areas

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