Literature DB >> 15929490

A case refort of Sandhoff disease.

Yie-Min Yun1, Su-Na Lee.   

Abstract

Sandhoff disease is a rare autosomal recessive metabolic disease presenting bilateral optic atrophy and a cherry red spot in the macula. This case report presents the characteristics of a patient with Sandhoff disease as assessed by ophthalmic, neuroimaging, and laboratory procedures. Ophthalmologic examination revealed that the patient could not fixate her eyes on objects nor follow moving targets. A pale optic disc and a cherry red spot in the macula were seen in both eyes. Low signal intensity at the thalamus and high signal intensity at the cerebral white matter were noted in a T2-weighted brain MR image. A lysosomal enzyme assay using fibroblasts showed the marked reduction of both total beta-hexosaminidases, A and B. Based on the above clinical manifestations and laboratory findings, we diagnosed the patient as having Sandhoff disease.

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Year:  2005        PMID: 15929490     DOI: 10.3341/kjo.2005.19.1.68

Source DB:  PubMed          Journal:  Korean J Ophthalmol        ISSN: 1011-8942


  7 in total

Review 1.  Decreased T2 signal in the thalami may be a sign of lysosomal storage disease.

Authors:  Taina Autti; Raimo Joensuu; Laura Aberg
Journal:  Neuroradiology       Date:  2007-03-03       Impact factor: 2.804

2.  P. Ala278Val mutation might cause a pathogenic defect in HEXB folding leading to the Sandhoff disease.

Authors:  Zahra Rahmani; Arsham Banisadr; Vadieh Ghodsinezhad; Mohsen Dibaj; Omid Aryani
Journal:  Metab Brain Dis       Date:  2022-10-03       Impact factor: 3.655

3.  Early changes in the apparent diffusion coefficient (ADC) in a mouse model of Sandhoff's disease occur prior to disease symptoms and behavioral deficits.

Authors:  Lingyun Hu; Yingying Sun; Laura E Villasana; Richard Paylor; Eric Klann; Robia G Pautler
Journal:  Magn Reson Med       Date:  2009-11       Impact factor: 4.668

4.  TSPO in a murine model of Sandhoff disease: presymptomatic marker of neurodegeneration and disease pathophysiology.

Authors:  Meredith K Loth; Judy Choi; Jennifer L McGlothan; Mikhail V Pletnikov; Martin G Pomper; Tomás R Guilarte
Journal:  Neurobiol Dis       Date:  2015-11-03       Impact factor: 5.996

5.  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

6.  Sandhoff Disease without Hepatosplenomegaly Due to Hexosaminidase B Gene Mutation.

Authors:  Vykuntaraju K Gowda; Raghavendraswami Amoghimath; Varun M Srinivasan; Maya Bhat
Journal:  J Pediatr Neurosci       Date:  2017 Jan-Mar

Review 7.  Abnormal Sphingolipid World in Inflammation Specific for Lysosomal Storage Diseases and Skin Disorders.

Authors:  Marta Moskot; Katarzyna Bocheńska; Joanna Jakóbkiewicz-Banecka; Bogdan Banecki; Magdalena Gabig-Cimińska
Journal:  Int J Mol Sci       Date:  2018-01-15       Impact factor: 5.923

  7 in total

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