Please use this identifier to cite or link to this item:
|Title:||Melkerrson-Rosenthal syndrome wilth cardiac involvement||Authors:||Chan, Y.C.
|Keywords:||Complete heart block
Cranial nerve palsy
Eye abduction limitation
|Issue Date:||2004||Citation:||Chan, Y.C., Ong, B.K.C., Wilder-Smith, E., Lee, Y.S., Wong, S.T., Lam, S.P. (2004). Melkerrson-Rosenthal syndrome wilth cardiac involvement. Journal of Clinical Neuroscience 11 (3) : 309-311. ScholarBank@NUS Repository.||Abstract:||Melkerrson-Rosenthal syndrome (MRS) is a granulomatous disease usually restricted to the orofacial region. We report a case of MRS in a 37-year-old Malay patient who presented with complete heart block on a background of recurrent oro-facial swelling and facial diplegia. Lip biopsy showed lymphohistocytic granulomatous inflammation typical for MRS. Extensive work-up excluded other causes of the complete heart block. To our knowledge, this is the first reported case of MRS affecting cardiac connective tissues and the first report of MRS in an ethnic Malay. We postulate granulomatous infiltration of the conductive tissues as the basis for the heart block. Another unusual feature of the case was the presence of left eye abduction limitation. © 2003 Elsevier Ltd. All rights reserved.||Source Title:||Journal of Clinical Neuroscience||URI:||http://scholarbank.nus.edu.sg/handle/10635/117774||ISSN:||09675868|
|Appears in Collections:||Staff Publications|
Show full item record
Files in This Item:
There are no files associated with this item.
checked on Mar 7, 2018
WEB OF SCIENCETM
checked on Dec 31, 2018
checked on Nov 8, 2019
Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.