Literature DB >> 20976786

Creutzfeldt-Jakob disease presenting as bulbar palsy.

Manoj Mittal1, Nancy Hammond, Kathrin Husmann, Abhijit Lele, Mamatha Pasnoor.   

Abstract

Creutzfeldt-Jakob disease (CJD) is a degenerative neurological disorder caused by a prion protein. The diagnosis may be challenging in unusual early presentations. A bulbar symptom as the initial complaint is a rare presentation for CJD, with only a few reports so far. These patients can be misdiagnosed with motor neuron disease or the Miller Fisher variant of Guillain-Barré syndrome. We describe a 69-year-old woman with CJD who presented with bulbar symptoms at the onset.

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Year:  2010        PMID: 20976786     DOI: 10.1002/mus.21849

Source DB:  PubMed          Journal:  Muscle Nerve        ISSN: 0148-639X            Impact factor:   3.217


  3 in total

1.  Isolated spasticity in sporadic Creutzfeldt-Jakob disease.

Authors:  Milena Marek; Thomas Klockgether; Horst Urbach; Inga Zerr; Hans Kretzschmar; Sebastian Paus
Journal:  J Neurol       Date:  2012-11-16       Impact factor: 4.849

2.  Creutzfeldt-Jakob disease with unusual presentation of peripheral neuropathy and ophthalmoplegia.

Authors:  Mais Arwani; Abhishek Purohit; Abdullah Haddad; Sandeep Rana
Journal:  Avicenna J Med       Date:  2018 Oct-Dec

Review 3.  Sporadic Creutzfeldt-Jakob disease: Real-Time Quaking Induced Conversion (RT-QuIC) assay represents a major diagnostic advance.

Authors:  Federico Angelo Cazzaniga; Edoardo Bistaffa; Chiara Maria Giulia De Luca; Giuseppe Bufano; Antonio Indaco; Giorgio Giaccone; Fabio Moda
Journal:  Eur J Histochem       Date:  2021-10-15       Impact factor: 3.188

  3 in total

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