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Journals / Türk Psikiyatri Dergisi / 2015 / Cilt: 26 - Sayı: 3

SUMMARY A Case of Sporadic Creutzfeldt-Jakob Disease That Developed With Psychiatric Symptoms

Psikiyatrik Bulgularla Başlayan Sporadik Creutzfeldt-Jakob Hastalığı Olgusu

Adile ÖZKAN
İlknur AYDIN CANTÜRK
Fatma CANDAN
Nihal IŞIK
Handan Işın ÖZIŞIK KARAMAN
Pages
213–220
DOI
—
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AI Summary & Key Takeaways

AI Insight
⚡ TL;DR(Too Long; Didn't Read)

The male patient who was diagnosed with CJD after dementia, ataxia, and myoclonus developed rapidly following psychiatric symptoms, was presented in order to draw attention to the onset with psychiatric symptoms in CJD.

📌 3 Key Takeaways

🎯
Objective & Hypothesis:Creutzfeldt-Jakob disease (CJD) is a fairly rare prion sickness characterized by rapidly progressive dementia and neuropsychiatric symptoms.
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Key Findings & Data:The diversity of clinical characteristics of the disease causes difficulties during diagnosis.
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Conclusion & Impact:The male patient who was diagnosed with CJD after dementia, ataxia, and myoclonus developed rapidly following psychiatric symptoms, was presented in order to draw attention to the onset with psychiatric symptoms in CJD.
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Domain Parameters

Abstract

Creutzfeldt-Jakob disease (CJD) is a fairly rare prion sickness characterized by rapidly progressive dementia and neuropsychiatric symptoms. The diversity of clinical characteristics of the disease causes difficulties during diagnosis. The first finding of the disease might be psychiatric symptoms. The male patient who was diagnosed with CJD after dementia, ataxia, and myoclonus developed rapidly following psychiatric symptoms, was presented in order to draw attention to the onset with psychiatric symptoms in CJD.

Özet

Creutzfeldt-Jakob hastalığı (CJH) oldukça nadir görülen hızlı seyirli de- mans ve nöropsikiyatrik belirtilerle seyreden bir prion hastalığıdır. Has- talığın klinik özelliklerinin çeşitlilik göstermesi tanı koyma aşamasında güçlük yaratır. Hastalığın ilk bulgusu psikiyatrik belirtiler olabilir. Psiki- yatrik belirtilerin ardından hızlı gelişen demans, ataksi, miyoklonus ile seyreden ve sonrasında CJH tanısı alan erkek hasta, CJH’da psikiyatrik belirtilerle başlangıca dikkat çekmek amacıyla sunulmuştur.

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Cite This Article

ÖZKAN, A., CANTÜRK, İ. A., CANDAN, F., IŞIK, N., KARAMAN, H. I. Ö. (2015). SUMMARY A Case of Sporadic Creutzfeldt-Jakob Disease That Developed With Psychiatric Symptoms. Türk Psikiyatri Dergisi, Cilt: 26 - Sayı: 3, 213–220. https://ajindex.com/articles/91705

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References (11)

  1. KAYNAKLAR Azorin JM, Donnet A, Dassa D ve ark. (1993) Creutzfeldt–Jacob disease misdiagnosed as depressive pseudo dementia. Compr Psychiatry 34:42–4. Bahn MM, Parchi P (1999) Abnormal diffusion-weighted magnetic resonance images in Creutzfeldt-Jakob disease. Arch Neurol 56:577-83.
  2. Brown P, Gibbs CJ, Rodgers-Johnson P ve ark. (1994) Human spongiform encephalopathy:the NIH series of 300 cases of experimentally transmitted disease. Ann Neurol 35:513-29.
  3. Brown P, Cathala F, Castaigne P ve ark. (1986) Creutzfeldt–Jacob disease: Clinical analysis of a consecutive series of 230 neuropathologically verified cases. Ann Neurol 20:597–602. Collins SJ, Sanchez-Juan P, Masters CL ve ark. (2006) Determinants of diagnostic investigation sensitivities across clinical spectrum of sporadic Creutzfeldt-Jakob disease. Brain 129:2278–87. Dervaux A, Laine H (2003) The psychiatric forms of Creutzfeldt-Jakob disease. Presse Med 32:1466-8.
  4. Finkenstaedt M, Szudra A, Zerr I ve ark. (1996) MR imaging of Creutzfeldt Jacob disease. Radiology 199:793-8.
  5. Glatzel M, Stoeck K, Seeger H ve ark. (2005) Human priondiseases: Molecular and clinical aspects. Arch Neurol 62:545–52. Green AJ (2002) Use of 14-3-3 in the diagnosis of Creutzfeldt- Jakob disease. Biochem Soc Trans 30:382-6.
  6. Hsich G, Kenney K, Gibbs CJ ve ark. (1996) The 14-3-3 brain protein in cerebrospinal fluid as a marker for transmissible spongiform encephalopathies. N Engl J Med 335:924-30.
  7. Johnson RT (2005) Prion diseases. Lancet Neurol 4:635–42. Keshavan MS, Lishman WA, Haghes JT (1987) Psychiatric presentation of Creutzfeldt–Jacob disease. A case report. Br J Psychiatry 151:260–3. Kurne A, Ertuğrul A, Yağcıoğlu EA ve ark. (2005) Creutzfeldt-Jakob Hastalığı: Psikiyatrik Belirtilerle Başlayan Bir Olgu. Turk Psikiyatri Derg 16:55-9.
  8. Mittal S, Farmer P, Kalina P ve ark. (2002) Correlation of diffusion- weighted magnetic resonance imaging with neuropathology in Creutzfeldt- Jakob disease. Arch Neurol 59:128-34.
  9. Shiga Y, Miyazawa K, Sato S ve ark. (2004) Diffusionweighted MRI abnormalities as an early diagnostic marker for Creutzfeldt-Jakob disease. Neurology 63: 443-9.
  10. Solvason HB, Harris B, Zeifert P ve ark. (2002) Psychological versus biological clinical interpretation: A patient with prion disease. Am J Psychiatry 159: 528–37. Ukisu R, Kushihashi T, Kitanosono T ve ark. (2005) Serial diffusionweighted MRI of Creutzfeldt-Jakob disease. Am J Roentgenol 184:560-6.
  11. Van Everbroeck B, Dobbeleir I, De Waele M ve ark. (2004) Differentia