Literature DB >> 2621550

Visual impairment in a case of juvenile Paget's disease with pseudoxanthoma elasticum: an eleven year follow up.

K W Sharif1, W M Doig, F P Kinsella.   

Abstract

An 11-year follow-up of a child presenting with Paget's disease of bone, and who subsequently developed pseudoxanthoma elasticum, is described. The influence of therapy on the ocular manifestations was disappointing. Calcitonin did not prevent the occurrence or progression of angioid streaks, and Argon laser photocoagulation of complicating subretinal neovascular membranes failed to prevent visual loss.

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Year:  1989        PMID: 2621550     DOI: 10.3928/0191-3913-19891101-13

Source DB:  PubMed          Journal:  J Pediatr Ophthalmol Strabismus        ISSN: 0191-3913            Impact factor:   1.402


  2 in total

1.  Juvenile paget's disease in an Iranian kindred with vitamin D deficiency and novel homozygous TNFRSF11B mutation.

Authors:  Forough Saki; Zohreh Karamizadeh; Shiva Nasirabadi; Steven Mumm; William H McAlister; Michael P Whyte
Journal:  J Bone Miner Res       Date:  2013-06       Impact factor: 6.741

2.  Juvenile Paget's Disease From Heterozygous Mutation of SP7 Encoding Osterix (Specificity Protein 7, Transcription Factor SP7).

Authors:  Michael P Whyte; Philippe M Campeau; William H McAlister; G David Roodman; Nori Kurihara; Angela Nenninger; Shenghui Duan; Gary S Gottesman; Vinieth N Bijanki; Homer Sedighi; Deborah J Veis; Steven Mumm
Journal:  Bone       Date:  2020-04-13       Impact factor: 4.398

  2 in total

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