Literature DB >> 14872044

Clinical features of Creutzfeldt-Jakob disease with V180I mutation.

K Jin1, Y Shiga, S Shibuya, K Chida, Y Sato, H Konno, K Doh-ura, T Kitamoto, Y Itoyama.   

Abstract

The authors describe the clinical features of Creutzfeldt-Jakob disease (CJD) with the causative point mutation at codon 180. The symptoms never started with visual or cerebellar involvement. The patients showed slower progression of the disease compared with sporadic CJD. They never showed periodic sharp and wave complexes in EEG. MRI demonstrated remarkable high-intensity areas with swelling in the cerebral cortex except for the medial occipital and cerebellar cortices. These characteristic MRI findings are an important clue for an accurate premortem diagnosis.

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Year:  2004        PMID: 14872044     DOI: 10.1212/01.wnl.0000106954.54011.80

Source DB:  PubMed          Journal:  Neurology        ISSN: 0028-3878            Impact factor:   9.910


  26 in total

1.  Diffusion-weighted and fluid-attenuated inversion recovery imaging in Creutzfeldt-Jakob disease: high sensitivity and specificity for diagnosis.

Authors:  Geoffrey S Young; Michael D Geschwind; Nancy J Fischbein; Jennifer L Martindale; Roland G Henry; Songling Liu; Ying Lu; Stephen Wong; Hong Liu; Bruce L Miller; William P Dillon
Journal:  AJNR Am J Neuroradiol       Date:  2005 Jun-Jul       Impact factor: 3.825

2.  Pathological progression of genetic Creutzfeldt-Jakob disease with a PrP V180I mutation.

Authors:  Akio Akagi; Yasushi Iwasaki; Maya Mimuro; Tetsuyuki Kitamoto; Masahito Yamada; Mari Yoshida
Journal:  Prion       Date:  2018-01-31       Impact factor: 3.931

3.  An autopsy-verified case of steroid-responsive encephalopathy with convulsion and a false-positive result from the real-time quaking-induced conversion assay.

Authors:  Yuichi Hayashi; Yasushi Iwasaki; Nobuaki Yoshikura; Takahiko Asano; Maya Mimuro; Akio Kimura; Katsuya Satoh; Tetsuyuki Kitamoto; Mari Yoshida; Takashi Inuzuka
Journal:  Prion       Date:  2017-07-27       Impact factor: 3.931

4.  Pathogenic mutations in the hydrophobic core of the human prion protein can promote structural instability and misfolding.

Authors:  Marc W van der Kamp; Valerie Daggett
Journal:  J Mol Biol       Date:  2010-10-07       Impact factor: 5.469

5.  Pathologic evidence that the T188R mutation in PRNP is associated with prion disease.

Authors:  Maria Carmela Tartaglia; Julie N Thai; Tricia See; Amy Kuo; Robert Harbaugh; Benjamin Raudabaugh; Ignazio Cali; Mamta Sattavat; Henry Sanchez; Stephen J DeArmond; Michael D Geschwind
Journal:  J Neuropathol Exp Neurol       Date:  2010-12       Impact factor: 3.685

6.  A Creutzfeldt-Jakob disease patient with V180I mutation survived for 16.5 years after diagnosis.

Authors:  Nayoung Ryoo; SangHak Yi; Seong Soo A An; Young Ho Park; SangYun Kim
Journal:  Acta Neurol Belg       Date:  2022-01-13       Impact factor: 2.396

7.  Rare V180I mutation in PRNP gene of a Chinese patient with Creutzfeldt-Jakob disease.

Authors:  Qi Shi; Xiao-Jing Shen; Wei Zhou; Kang Xiao; Xiao-Mei Zhang; Bao-Yun Zhang; Xiao-Ping Dong
Journal:  Prion       Date:  2014       Impact factor: 3.931

8.  Familial Creutzfeldt-Jakob disease with a V180I mutation: comparative analysis with pathological findings and diffusion-weighted images.

Authors:  Kazuo Mutsukura; Katsuya Satoh; Susumu Shirabe; Itsuro Tomita; Takayasu Fukutome; Minoru Morikawa; Masachika Iseki; Kensuke Sasaki; Yusei Shiaga; Tetsuyuki Kitamoto; Katsumi Eguchi
Journal:  Dement Geriatr Cogn Disord       Date:  2009-12-30       Impact factor: 2.959

9.  Familial Creutzfeldt-Jakob disease with V180I mutation.

Authors:  Tae-Il Yang; Dae-Soo Jung; Bo-Young Ahn; Byung-Hoon Jeong; Han-Jeong Cho; Yong-Sun Kim; Duk L Na; Michael D Geschwind; Eun-Joo Kim
Journal:  J Korean Med Sci       Date:  2010-06-16       Impact factor: 2.153

10.  IFRD1 is a candidate gene for SMNA on chromosome 7q22-q23.

Authors:  Zoran Brkanac; David Spencer; Jay Shendure; Peggy D Robertson; Mark Matsushita; Tiffany Vu; Thomas D Bird; Maynard V Olson; Wendy H Raskind
Journal:  Am J Hum Genet       Date:  2009-04-30       Impact factor: 11.025

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