Literature DB >> 18536898

Systemic onset juvenile idiopathic arthritis--its unusual presentation.

J B Ghosh1, Dipankar Gupta, Nibedita Chattopadhyay.   

Abstract

We report a case of systemic onset juvenile idiopathic arthritis (SOJIA), the manifestations of which started with fever and skin rash followed by arthritis within neonatal age. Such presentation is extremely rare in the newborn. After exclusion of closely mimicking conditions like congenital infections, neonatal onset multisystem inflammatory disease (NOMID), neonatal; lupus erythematosus (NLE) diagnosis of SOJIA may be entertained even in a neonate where arthritis, fever and rash are the presenting features.

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Year:  2008        PMID： 18536898     DOI： 10.1007/s12098-008-0046-1

Source DB:  PubMed          Journal:  Indian J Pediatr        ISSN： 0019-5456            Impact factor:   5.319


  6 in total

1.  Allan-Herndon syndrome. I. Clinical studies.

Authors:  R E Stevenson; H O Goodman; C E Schwartz; R J Simensen; W T McLean; C N Herndon
Journal:  Am J Hum Genet       Date:  1990-09       Impact factor: 11.025

2.  Allan-Herndon-Dudley syndrome and the monocarboxylate transporter 8 (MCT8) gene.

Authors:  Charles E Schwartz; Melanie M May; Nancy J Carpenter; R Curtis Rogers; Judith Martin; Martin G Bialer; Jewell Ward; Javier Sanabria; Silvana Marsa; James A Lewis; Roberto Echeverri; Herbert A Lubs; Kytja Voeller; Richard J Simensen; Roger E Stevenson
Journal:  Am J Hum Genet       Date:  2005-05-11       Impact factor: 11.025

3.  Decreased cellular uptake and metabolism in Allan-Herndon-Dudley syndrome (AHDS) due to a novel mutation in the MCT8 thyroid hormone transporter.

Authors:  C M C Maranduba; E C H Friesema; F Kok; M H A Kester; J Jansen; A L Sertié; M R Passos-Bueno; T J Visser
Journal:  J Med Genet       Date:  2005-06-24       Impact factor: 6.318

4.  Allan-Herndon-Dudley syndrome: clinical and linkage studies on a second family.

Authors:  M G Bialer; L Lawrence; R E Stevenson; G Silverberg; M K Williams; J F Arena; H A Lubs; C E Schwartz
Journal:  Am J Med Genet       Date:  1992 Apr 15-May 1

5.  Association between mutations in a thyroid hormone transporter and severe X-linked psychomotor retardation.

Authors:  Edith C H Friesema; Annette Grueters; Heike Biebermann; Heiko Krude; Arpad von Moers; Maarten Reeser; Timothy G Barrett; Edna E Mancilla; Johan Svensson; Monique H A Kester; George G J M Kuiper; Sahila Balkassmi; André G Uitterlinden; Josef Koehrle; Patrice Rodien; Andrew P Halestrap; Theo J Visser
Journal:  Lancet       Date:  2004 Oct 16-22       Impact factor: 79.321

6.  A novel syndrome combining thyroid and neurological abnormalities is associated with mutations in a monocarboxylate transporter gene.

Authors:  Alexandra M Dumitrescu; Xiao-Hui Liao; Thomas B Best; Knut Brockmann; Samuel Refetoff
Journal:  Am J Hum Genet       Date:  2003-12-05       Impact factor: 11.025
  6 in total
  1 in total

Review 1.  Autoinflammation: From monogenic syndromes to common skin diseases.

Authors:  Tien V Nguyen; Edward W Cowen; Kieron S Leslie
Journal:  J Am Acad Dermatol       Date:  2013-02-28       Impact factor: 11.527
  1 in total

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