1.
Indian J Pediatr
;
2010 Mar; 77(3): 339
Article
in English
| IMSEAR
| ID: sea-142540
2.
Indian Pediatr
;
2007 Dec; 44(12): 933-6
Article
in English
| IMSEAR
| ID: sea-14953
ABSTRACT
CINCA syndrome is a genetic disorder characterized by early onset of recurrent fever, rash, progressive articular and neurological involvement. We report a 7-year-old girl with CINCA syndrome with an infrequent manifestation of retinal vasculitis and a relative paucity of neurological signs. She had a de novo F309S mutation in exon 3 of CIAS1 gene on chromosome 1.This is the first report of this entity from India.
Subject(s)
Age Factors , Arthritis/drug therapy , Azathioprine/therapeutic use , Carrier Proteins/genetics , Child , Chronic Disease , Erythema/drug therapy , Female , Fever/drug therapy , Humans , Mutation , Nervous System Diseases/drug therapy , Prednisolone/therapeutic use , Syndrome
3.
Indian Pediatr
;
2007 Jan; 44(1): 47
Article
in English
| IMSEAR
| ID: sea-13830
4.
Indian J Pediatr
;
2006 Jun; 73(6): 545; author reply 546
Article
in English
| IMSEAR
| ID: sea-80931