Literature DB >> 8870920

Juvenile rheumatoid arthritis in velo-cardio-facial syndrome: coincidence or unusual complication?

S A Rasmussen1, C A Williams, E M Ayoub, J W Sleasman, B A Gray, A Bent-Williams, H J Stalker, R T Zori.   

Abstract

We report on two patients with velo-cardio-facial syndrome (VCFS) and juvenile rheumatoid arthritis (JRA). The first, a 9-year-old girl, presented with microcephaly, characteristic face, congenital heart disease, and velopharyngeal insufficiency. Fluorescence in situ hybridization (FISH) study showed deletion of D22S75 (N25), confirming the diagnosis of VCFS. At age 7, she developed joint pain, and polyarticular JRA was diagnosed. Awareness of this case led to the subsequent diagnosis of VCFS (also confirmed by FISH) in another, unrelated 12-year-old girl with characteristic face, hypernasal speech, and obesity. JRA was first diagnosed in this case at age 5 years, and she subsequently developed severe polyarticular disease. Neither patient had clinical or laboratory evidence of immunodeficiency. This observation represents the first report of the association of JRA with VCFS and raises the question of whether this is a coincidental association or a rare complication of this condition.

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Year:  1996        PMID: 8870920     DOI: 10.1002/(SICI)1096-8628(19960906)64:4<546::AID-AJMG4>3.0.CO;2-N

Source DB:  PubMed          Journal:  Am J Med Genet        ISSN: 0148-7299


  10 in total

1.  Radial aplasia and chromosome 22q11 deletion.

Authors:  M C Digilio; A Giannotti; B Marino; A M Guadagni; M Orzalesi; B Dallapiccola
Journal:  J Med Genet       Date:  1997-11       Impact factor: 6.318

2.  Spectrum of clinical features associated with interstitial chromosome 22q11 deletions.

Authors:  M Di Rocco; A Buocompagni; P Picco; S Vignola; C Borrone; G Gimelli
Journal:  J Med Genet       Date:  1998-04       Impact factor: 6.318

Review 3.  Immunological aspects of 22q11.2 deletion syndrome.

Authors:  A R Gennery
Journal:  Cell Mol Life Sci       Date:  2011-10-09       Impact factor: 9.261

4.  Longitudinal analysis of lymphocyte function and numbers in the first year of life in chromosome 22q11.2 deletion syndrome (DiGeorge syndrome/velocardiofacial syndrome).

Authors:  K E Sullivan; D McDonald-McGinn; D A Driscoll; B S Emanuel; E H Zackai; A F Jawad
Journal:  Clin Diagn Lab Immunol       Date:  1999-11

5.  Uveitis in DiGeorge syndrome: a case of autoimmune ocular inflammation in a patient with deletion 22q11.2.

Authors:  Chloe Gottlieb; Zhuqing Li; Gulbu Uzel; Robert B Nussenblatt; H Nida Sen
Journal:  Ophthalmic Genet       Date:  2010-03       Impact factor: 1.803

6.  Whole-Genome Sequencing and Integrative Genomic Analysis Approach on Two 22q11.2 Deletion Syndrome Family Trios for Genotype to Phenotype Correlations.

Authors:  Jonathan H Chung; Jinlu Cai; Barrie G Suskin; Zhengdong Zhang; Karlene Coleman; Bernice E Morrow
Journal:  Hum Mutat       Date:  2015-07-02       Impact factor: 4.878

7.  A case of juvenile idiopathic polyarticular arthritis complicated by IgA deficiency in 22q11 deletion syndrome.

Authors:  Satoshi Sato; Hisashi Kawashima; Kazunori Suzuki; Ryuhei Nagao; Kazumitsu Tsuyuki; Akinori Hoshika
Journal:  Rheumatol Int       Date:  2009-12-11       Impact factor: 2.631

8.  Juvenile rheumatoid arthritis and del(22q11) syndrome: a non-random association.

Authors:  A Verloes; C Curry; M Jamar; C Herens; P O'Lague; J Marks; P Sarda; P Blanchet
Journal:  J Med Genet       Date:  1998-11       Impact factor: 6.318

9.  Association of juvenile idiopathic arthritis and digeorge syndrome; a case report.

Authors:  Farhad Salehzadeh; Amin Bagheri
Journal:  Iran J Pediatr       Date:  2014-06       Impact factor: 0.364

Review 10.  Immunodeficiency in DiGeorge Syndrome and Options for Treating Cases with Complete Athymia.

Authors:  E Graham Davies
Journal:  Front Immunol       Date:  2013-10-31       Impact factor: 7.561

  10 in total

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