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

Fingerprint Dive into the research topics of 'Aicardi-Goutieres syndrome in siblings'. Together they form a unique fingerprint.

Cite this

@article{9beead005f9f49aa887bc7f359e04e4a,

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",

year = "2001",

language = "English",

volume = "16",

pages = "759--761",

journal = "Journal of Child Neurology",

issn = "0883-0738",

publisher = "SAGE Publications Inc.",

number = "10",

}

TY - JOUR

T1 - Aicardi-Goutieres syndrome in siblings

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.

UR - http://www.scopus.com/inward/record.url?scp=0035212482&partnerID=8YFLogxK

UR - http://www.scopus.com/inward/citedby.url?scp=0035212482&partnerID=8YFLogxK

M3 - Article

C2 - 11669350

AN - SCOPUS:0035212482

VL - 16

SP - 759

EP - 761

JO - Journal of Child Neurology

JF - Journal of Child Neurology

SN - 0883-0738

IS - 10

ER -

Aicardi-Goutieres syndrome in siblings

Abstract

ASJC Scopus subject areas

Other files and links

Cite this