Literature DB >> 1789967

A case of progressive hemifacial atrophy with uveitis and retinal vasculitis.

K Ong1, F A Billson, D S Pathirana, P Clifton-Bligh.   

Abstract

Parry Romberg syndrome is a rare disorder characterised by progressive hemifacial atrophy that is usually unilateral, involving the skin, subcutaneous tissue, and subsequently the muscle, cartilage and bone. Previous cases with various ocular manifestations have been reported. A case of Parry Romberg syndrome with retinal vasculitis is reported.

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Year:  1991        PMID: 1789967     DOI: 10.1111/j.1442-9071.1991.tb00675.x

Source DB:  PubMed          Journal:  Aust N Z J Ophthalmol        ISSN: 0814-9763


  4 in total

1.  Progressive hemifacial atrophy. A natural history study.

Authors:  M T Miller; M A Spencer
Journal:  Trans Am Ophthalmol Soc       Date:  1995

Review 2.  Progressive hemifacial atrophy: a review.

Authors:  Stanislav N Tolkachjov; Nirav G Patel; Megha M Tollefson
Journal:  Orphanet J Rare Dis       Date:  2015-04-01       Impact factor: 4.123

3.  Parry Romberg syndrome: A case report and discussion.

Authors:  Ramasamy Madasamy; Muruganandhan Jayanandan; Uma Revathy Adhavan; Sivakumar Gopalakrishnan; Lodd Mahendra
Journal:  J Oral Maxillofac Pathol       Date:  2012-09

4.  Parry Romberg syndrome with a wide range of ocular manifestations: a case report.

Authors:  Antonio Maria Fea; Vittoria Aragno; Cristina Briamonte; Mauro Franzone; Davide Putignano; Federico Maria Grignolo
Journal:  BMC Ophthalmol       Date:  2015-09-05       Impact factor: 2.209

  4 in total

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