Literature DB >> 623187

Ocular manifestations of group A Niemann-Pick disease.

D S Walton, R M Robb, A C Crocker.   

Abstract

Four infants with Group A Niemann-Pick disease had similar ocular abnormalities secondary to this systemic disease. Each child demonstrated corneal opacification, brown discoloration of the anterior lens capsule, and retinal opacification with a macular cherry-red spot. These abnormalities were seen in each child during the first year of life and appeared stable. Recognition of this combination of ocular defects facilitates early identification of patients with Group A infantile Niemann-Pick disease.

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Year:  1978        PMID: 623187     DOI: 10.1016/s0002-9394(14)75945-8

Source DB:  PubMed          Journal:  Am J Ophthalmol        ISSN: 0002-9394            Impact factor:   5.258


  3 in total

Review 1.  Beyond the cherry-red spot: Ocular manifestations of sphingolipid-mediated neurodegenerative and inflammatory disorders.

Authors:  Hui Chen; Annie Y Chan; Donald U Stone; Nawajes A Mandal
Journal:  Surv Ophthalmol       Date:  2013-09-05       Impact factor: 6.048

2.  A new variant of sphingomyelinase deficiency (Niemann-Pick): visceromegaly, minimal neurological lesions and low in vivo degradation rate of sphingomyelin.

Authors:  M Elleder; J Nevoral; V Spicáková; H Hyniová; J Kraus; J Krásný; M T Vanier
Journal:  J Inherit Metab Dis       Date:  1986       Impact factor: 4.982

3.  Oculo-neural involvement in an enzymatically proven case of Niemann-Pick disease type B.

Authors:  G Hammersen; H C Oppermann; E Harms; K Blassmann; K Harzer
Journal:  Eur J Pediatr       Date:  1979-10       Impact factor: 3.183

  3 in total

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