Taysachs disease- A case report
Abstract
Taysachs disease is one of the GM2 gangliosidosis seen commonly in askanesian jews.We report the case of an Indian infant with this condition.
Full Text:
PDFReferences
Nelson Text book of Pediatrics, 19th edition, By Robert M. Kliegman et al
Am J Hum Genet. 1995; 57:A57. By Eng, CM, Burgert, TS, Schecter, C, et al, Title: Multiplex
genetic testing in the Ashkenazi Jewish population
Kaback, Michael M (December 2000). "Population-based genetic screening for reproductive
counseling: the Tay–Sachs disease model". European Journal of Pediatrics 159 (Suppl 3):
S192–S195.
http://www.ncbi.nlm.nih.gov/pubmedhealth/PMH0002390/ , A.D.A.M. Medical Encyclopedia.,Last
reviewed: November 2, 2012. Accessed on 15th october 2013
CLINICAL PEDIATRIC NEUROLOGY, A Signs and symptoms Approach by Gerald M. Fenichel
paAge 129.
www.nhs.uk/Conditions/Tay-Sachs-disease/Pages/Treatment.aspx
Refbacks
- There are currently no refbacks.
This work is licensed under a Creative Commons Attribution-NoDerivatives 4.0 International License.
An initiative of The Tamil Nadu Dr M.G.R. Medical University