Literature DB >> 7258948

Familial pars planitis.

J J Augsburger, W H Annesley, R C Sergott, N T Felberg, J H Bowman, L A Raymond.   

Abstract

Pars planitis has rarely been noted to occur in more than one member of a family. We report the occurrence of this disorder in more than one member of two unrelated families. The affected members of one of these families included a 37-year-old woman and three of her six children. The affected members of the other family were two teenaged brothers. No specific cause for the familial clustering of pars planitis has been identified in the affected members of these families.

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Year:  1981        PMID: 7258948

Source DB:  PubMed          Journal:  Ann Ophthalmol        ISSN: 0003-4886


  4 in total

1.  HLA typing of a Hong Kong Chinese family with intermediate uveitis.

Authors:  A C Browning; D Calladine; N Collins; A W Harmer; W M Amoaku
Journal:  Br J Ophthalmol       Date:  2006-05       Impact factor: 4.638

2.  Clinical and immunopathological studies of pars planitis in a family.

Authors:  R P Wetzig; C C Chan; R B Nussenblatt; A G Palestine; D O Mazur; K K Mittal
Journal:  Br J Ophthalmol       Date:  1988-01       Impact factor: 4.638

3.  Dominant exudative vitreoretinopathy and other vascular developmental disorders of the peripheral retina.

Authors:  C E van Nouhuys
Journal:  Doc Ophthalmol       Date:  1982-09-23       Impact factor: 2.379

4.  Tumor necrosis factor polymorphisms associated with tumor necrosis factor production influence the risk of idiopathic intermediate uveitis.

Authors:  Denize Atan; Jarka Heissigerova; Lucia Kuffová; Aideen Hogan; Dara J Kilmartin; John V Forrester; Jeff L Bidwell; Andrew D Dick; Amanda J Churchill
Journal:  Mol Vis       Date:  2013-01-28       Impact factor: 2.367

  4 in total

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