Literature DB >> 11056783

Sandhoff disease--a case report of 3 siblings and a review of potential therapies.

S K Tay1, P S Low, H T Ong, K Y Loke.   

Abstract

INTRODUCTION: Sandhoff disease is a GM2 gangliosidosis that may present within the first 6 months of life with developmental regression. This is the first report of a pedigree from Southeast Asia. CLINICAL PICTURE: All the affected siblings presented in the first year of life with developmental regression, spasticity, seizures and loss of vision. The diagnosis was confirmed by an enzymatic deficiency in both beta-hexosaminidase A and B.
CONCLUSION: As the disorder is autosomal recessive, and no curative therapy is currently available, genetic counselling is necessary to prevent the burden of this devastating disease. We review the potential strategies of treatment for Sandhoff disease.

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Year:  2000        PMID: 11056783

Source DB:  PubMed          Journal:  Ann Acad Med Singapore        ISSN: 0304-4602            Impact factor:   2.473


  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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