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01 · ABSTRACT

Abstract

Creutzfeldt-Jakob disease (CJD) is a rare neurodegenerative disease of undetermined etiology, In Creutzfeldt-Jakob syndrome the symptomatology is quite variable and it  consist of predominantly progressive dementia with a rapid onset, myoclonus, and also cerebellar, pyramidal, extrapyramidal and visual signs, the evolution of this disease is uniformly fatal, most patients die within 12 months, we present a case of a 72 year old women, who was admitted for a status epilepticus, She was later diagnosed with sporadic CJD.

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02 · PUBLICATION RECORD

Article details

JournalMedical Research Archives
IssueVol 11 No 8 (2023): August Issue, Vol.11, Issue 8
SectionCase Reports
Published30 August 2023
DOI10.18103/mra.v11i8.3932
ISSN2375-1924
03 · RIGHTS & REUSE

Rights & reuse

This article is published under a Creative Commons Attribution License (CC BY 3.0) and may be shared or distributed by anyone as long as attribution is given to the journal.

Authors & affiliations

ME

Mabchour E

1. Departement of intensive care medicine, ibn rochd university hospital, faculty of medicine and pharmacy of casablanca, Hassan 2 university, Casablanca, Morocco.

MO

Maghrabi O

1. Departement of intensive care medicine, ibn rochd university hospital, faculty of medicine and pharmacy of casablanca, Hassan 2 university, Casablanca, Morocco.

MW

Machrouh W

1. Departement of intensive care medicine, ibn rochd university hospital, faculty of medicine and pharmacy of casablanca, Hassan 2 university, Casablanca, Morocco.

CB

Charra B

head of department of medical intensive care, ibn rochd university hospital

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