HUNTINGTON HASTALIĞI: İKİ OLGU

Cilt: 45 Sayı: 2 1 Haziran 2006
  • Nurşen Kömürcülü
  • Aysun İnce
  • Ebru Bakar
  • Hikmet Yılmaz
  • İnanç Karapolat
  • Deniz Selçuki
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CASE REPORT: TWO PATIENTS WITH HUNTINGTON'S DISEASE

Abstract

Huntington's disease is an autosomal dominantly transmitted, progressive neuro-degenerative disease which presents itself with motor, psychiactric and cognitive dysfunction. Diagnosis of genetically transmitted disease is important in many aspects. 56 year-old female and 61year-old male patients referred to the hospital with compliants of forgetfulness, involuntary movements and depressive-like symtoms. The female patients cranial magnetic resonans imagining (MRI) showed diffuse atrophy and the male patient's MRI was notable for fokal areas of atrophies mainly in the caudate and putamen nuclei. In PET( Positron emission tomography) examination low methabolic activity of FDG in the caudate nucleus of both patients supported the diagnosis the genetic results of N19/Exp43 CAG. The clinical significance of PET study was stated in two genetically diafnascd cases with, Huntington's diseas.

Keywords

Ayrıntılar

Birincil Dil

Türkçe

Konular

-

Bölüm

-

Yazarlar

Nurşen Kömürcülü

Aysun İnce

Ebru Bakar

Hikmet Yılmaz

İnanç Karapolat

Deniz Selçuki

Yayımlanma Tarihi

1 Haziran 2006

Gönderilme Tarihi

1 Haziran 2006

Kabul Tarihi

-

Yayımlandığı Sayı

Yıl 1970 Cilt: 45 Sayı: 2

Kaynak Göster

Vancouver
1.Nurşen Kömürcülü, Aysun İnce, Ebru Bakar, Hikmet Yılmaz, İnanç Karapolat, Deniz Selçuki. HUNTINGTON HASTALIĞI: İKİ OLGU. ETD [Internet]. 01 Haziran 2006;45(2):139-43. Erişim adresi: https://izlik.org/JA58BM75HP

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