Literature DB >> 6639422

Macula halo syndrome. Variant of Niemann-Pick disease.

D G Cogan, F C Chu, J A Barranger, R E Gregg.   

Abstract

The macula halo syndrome is the name proposed to describe patients with a unique ring-form opacity about the foveolas and a histiocytic storage disease. Since sphingomyelinase deficiency has now been found in the three patients in whom it was sought (including two in the present report), the entity may be classified as a variant of Niemann-Pick disease. A secondary hyperlipidemia may also be present. The macula halos consisting of symmetric crystalloid opacities with little or no visual impairment are pathognomonic of the entity.

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Year:  1983        PMID: 6639422     DOI: 10.1001/archopht.1983.01040020700005

Source DB:  PubMed          Journal:  Arch Ophthalmol        ISSN: 0003-9950


  3 in total

1.  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

2.  Niemann-Pick disease: sixteen-year follow-up of allogeneic bone marrow transplantation in a type B variant.

Authors:  S Victor; J B S Coulter; G T N Besley; I Ellis; R J Desnick; E H Schuchman; A Vellodi
Journal:  J Inherit Metab Dis       Date:  2003       Impact factor: 4.982

3.  A family with visceral course of Niemann-Pick disease, macular halo syndrome and low sphingomyelin degradation rate.

Authors:  W Sperl; G Bart; M T Vanier; H Christomanou; I Baldissera; E Steichen-Gersdorf; E Paschke
Journal:  J Inherit Metab Dis       Date:  1994       Impact factor: 4.982

  3 in total

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