Literature DB >> 2191759

Corneal changes in Tay-Sachs disease.

M Ghosh1, W S Hunter, C Wedge.   

Abstract

Tay-Sachs disease is a well-known inherited disease leading to an accumulation of gangliosides in the brain and retina. Our report is based on a case of Tay-Sachs disease in a non-Jewish infant where pathologic changes were noted in corneal endothelium as well as in the retina.

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Year:  1990        PMID： 2191759

Source DB:  PubMed          Journal:  Can J Ophthalmol        ISSN： 0008-4182            Impact factor:   1.882


  2 in total

1.  GM2-Gangliosidosis (Sandhoff and Tay Sachs disease): Diagnosis and Neuroimaging Findings (An Iranian Pediatric Case Series).

Authors:  Parvaneh Karimzadeh; Narjes Jafari; Habibeh Nejad Biglari; Sayena Jabbeh Dari; Farzad Ahmad Abadi; Mohammad-Reza Alaee; Hamid Nemati; Sasan Saket; Seyed Hasan Tonekaboni; Mohammad-Mahdi Taghdiri; Mohammad Ghofrani
Journal:  Iran J Child Neurol       Date:  2014

2.  Ophthalmologic Findings in Patients with Neuro-metabolic Disorders.

Authors:  Narjes Jafari; Karl Golnik; Mansoor Shahriari; Parvaneh Karimzadeh; Sayena Jabbehdari
Journal:  J Ophthalmic Vis Res       Date:  2018 Jan-Mar
  2 in total

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