Literature DB >> 15590544

Progressive visual loss in a child with Parry-Romberg syndrome.

Thomas A Finley1, R Michael Siatkowski.   

Abstract

Progressive hemifacial atrophy in Parry-Romberg syndrome is associated with a wide variety of ophthalmologic findings. Progressive visual loss, especially in the first decade, is rare in this condition. We present a young girl originally felt to have linear scleroderma and anisometropic amblyopia, who was eventually diagnosed with Parry-Romberg syndrome as the cause of her cutaneous and ophthalmologic findings.

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Year:  2004        PMID: 15590544     DOI: 10.1080/08820530490891139

Source DB:  PubMed          Journal:  Semin Ophthalmol        ISSN: 0882-0538            Impact factor:   1.975


  2 in total

Review 1.  The central nervous system manifestations of localized craniofacial scleroderma: a study of 10 cases and literature review.

Authors:  Ezekiel Maloney; Sarah J Menashe; Ramesh S Iyer; Sarah Ringold; Amit K Chakraborty; Gisele E Ishak
Journal:  Pediatr Radiol       Date:  2018-07-03

2.  A significant proportion of children with morphea en coup de sabre and Parry-Romberg syndrome have neuroimaging findings.

Authors:  Yvonne E Chiu; Sheetal Vora; Eun-Kyung M Kwon; Mohit Maheshwari
Journal:  Pediatr Dermatol       Date:  2012 Nov-Dec       Impact factor: 1.588

  2 in total

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