Literature DB >> 7850271

The blinding mechanisms of incontinentia pigmenti.

M F Goldberg1.   

Abstract

The ocular and cerebral abnormalities associated with incontinentia pigmenti, an X-linked dominant disease with characteristic cutaneous features, are far worse than the name would indicate. Although some patients have normal vision, total blindness or permanent visual deficiency may occur. Retinal vascular abnormalities, involving the periphery as well as the macula, appear to represent the primary disease process in the eye. Retinal detachment may then ensue, due to mechanisms that seem analogous to those of retinopathy of prematurity. Optic nerve atrophy and occipital lobe infarction are additional causes of severe visual dysfunction in some patients. For the first time, neonatal infarction of the macula is documented in this disease. The purpose of this report is to describe the visually disabling ocular and cerebral manifestations in five selected cases of incontinentia pigmenti.

Entities:  

Mesh:

Year:  1994        PMID: 7850271

Source DB:  PubMed          Journal:  Ophthalmic Genet        ISSN: 1381-6810            Impact factor:   1.803


  3 in total

1.  Structural Abnormalities of the Inner Macula in Incontinentia Pigmenti.

Authors:  Jacob Basilius; Marielle P Young; Timothy C Michaelis; Ronald Hobbs; Glen Jenkins; M Elizabeth Hartnett
Journal:  JAMA Ophthalmol       Date:  2015-09       Impact factor: 7.389

2.  Predominant exudative retinopathy in incontinentia pigmenti and clinical course after peripheral laser photocoagulation.

Authors:  Gaurav Sanghi; Mangat R Dogra; Munni Ray; Amod Gupta
Journal:  Indian J Ophthalmol       Date:  2011 May-Jun       Impact factor: 1.848

3.  Low vision due to cerebral visual impairment: differentiating between acquired and genetic causes.

Authors:  Daniëlle G M Bosch; F Nienke Boonstra; Michèl A A P Willemsen; Frans P M Cremers; Bert B A de Vries
Journal:  BMC Ophthalmol       Date:  2014-05-01       Impact factor: 2.209

  3 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.