CREUTZFELDT-JACOB DISEASE: A CASE REPORT

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SARAF PAYAM; GHAJARZADEH MAHSA; SALARIAN BABAK

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Journal Paper

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Journal: ACTA MEDICA IRANICA Year:2014 | Volume:52 | Issue:6 Page(s): 488-489

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Information Journal Paper

Title

CREUTZFELDT-JACOB DISEASE: A CASE REPORT

Author(s)

SARAF PAYAM | GHAJARZADEH MAHSA | SALARIAN BABAK | Issue Writer Certificate

Keywords

CREUTZFELDT-JACOB DISEASE

MAGNETIC RESONANCE IMAGING

ELECTROENCEPHALOGRAPHY

Abstract

CREUTZFELDT-JACOB DISEASE is a prion disease which has a wide range of clinical presentations. Its diagnosis is not simple and clinical manifestation along with EEG, MR imaging findings and cerebrospinal fluid (CSF) analysis should be considered for a definite diagnosis. A-50-year-old woman referred with cognitive impairment, myoclonic jerks, mutism and difficulty in swallowing to our clinic. EEG (Electroencephalography) results showed bilaterally periodic sharp and slow-wave discharges. Protein 14-3-3 in CSF was detected. MAGNETIC RESONANCE IMAGING (MRI) findings revealed hyperintensity of the caudate and putamen in diffusion-weighted imaging (DWI), T2 Weighted (T2W) sequences and Fluid-attenuated inversion-recovery (FLAIR) images. Patients who have progressive dementia should be evaluated by means of MR imaging and CSF analysis for CJD specific proteins should be considered.

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APA: Copy

SARAF, PAYAM, GHAJARZADEH, MAHSA, & SALARIAN, BABAK. (2014). CREUTZFELDT-JACOB DISEASE: A CASE REPORT. ACTA MEDICA IRANICA, 52(6), 488-489. SID. https://sid.ir/paper/278628/en

Vancouver: Copy

SARAF PAYAM, GHAJARZADEH MAHSA, SALARIAN BABAK. CREUTZFELDT-JACOB DISEASE: A CASE REPORT. ACTA MEDICA IRANICA[Internet]. 2014;52(6):488-489. Available from: https://sid.ir/paper/278628/en

IEEE: Copy

PAYAM SARAF, MAHSA GHAJARZADEH, and BABAK SALARIAN, “CREUTZFELDT-JACOB DISEASE: A CASE REPORT,” ACTA MEDICA IRANICA, vol. 52, no. 6, pp. 488–489, 2014, [Online]. Available: https://sid.ir/paper/278628/en

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