Access the full text.
Sign up today, get DeepDyve free for 14 days.
Loading next page...
/lp/wiley/proteinuria-in-neuronal-intranuclear-inclusion-disease-SW01hBugrE
References (8)
-
R. Lindenberg, L. Rubinstein, M. Herman, G. Haydon (1968)
A light and electron microscopy study of an unusual widespread nuclear inclusion body diseaseActa Neuropathologica, 10
-
J. Sone, F. Tanaka, H. Koike, A. Inukai, M. Katsuno, Mari Yoshida, Hirohisa Watanabe, G. Sobue (2011)
Skin biopsy is useful for the antemortem diagnosis of neuronal intranuclear inclusion diseaseNeurology, 76
-
J. Sone, N. Hishikawa, H. Koike, N. Hattori, M. Hirayama, M. Nagamatsu, M. Yamamoto, F. Tanaka, M. Yoshida, Y. Hashizume, H. Imamura, E. Yamada, G. Sobue (2005)
Neuronal intranuclear hyaline inclusion disease showing motor-sensory and autonomic neuropathyNeurology, 65
-
J. Sone, Naoyuki Kitagawa, E. Sugawara, Masaaki Iguchi, R. Nakamura, H. Koike, Y. Iwasaki, Mari Yoshida, Tatsuya Takahashi, S. Chiba, M. Katsuno, F. Tanaka, G. Sobue (2013)
Neuronal intranuclear inclusion disease cases with leukoencephalopathy diagnosed via skin biopsyJournal of Neurology, Neurosurgery & Psychiatry, 85
-
F. Goutières, J. Mikol, J. Aicardi (1990)
Neuronal intranuclear inclusion disease in a child: Diagnosis by rectal biopsyAnnals of Neurology, 27
-
J. Sone, K. Mori, T. Inagaki, Ryu Katsumata, S. Takagi, S. Yokoi, Kunihiko Araki, Toshiyasu Kato, Tomohiko Nakamura, H. Koike, H. Takashima, A. Hashiguchi, Y. Kohno, T. Kurashige, M. Kuriyama, Y. Takiyama, M. Tsuchiya, Naoyuki Kitagawa, M. Kawamoto, H. Yoshimura, Yutaka Suto, H. Nakayasu, N. Uehara, H. Sugiyama, Makoto Takahashi, N. Kokubun, T. Konno, M. Katsuno, F. Tanaka, Y. Iwasaki, Mari Yoshida, G. Sobue (2016)
Clinicopathological features of adult-onset neuronal intranuclear inclusion diseaseBrain, 139
-
J. Takahashi‐Fujigasaki, Yuta Nakano, A. Uchino, S. Murayama (2016)
Adult‐onset neuronal intranuclear hyaline inclusion disease is not rare in older adultsGeriatrics & Gerontology International, 16
-
R. Lindenberg, L. Rubinstein, M. Herman, G. Haydon (1968)
A light and electron microscopy study of an unusual widespread nuclear inclusion body disease. A possible residuum of an old herpesvirus infection.Acta neuropathologica, 10 1
- Publisher
- Wiley
- Copyright
- Copyright © 2018 Japanese Society of Neurology and John Wiley & Sons Australia, Ltd
- ISSN
- 2049-4173
- eISSN
- 2049-4173
- DOI
- 10.1111/ncn3.12182
- Publisher site
- See Article on Publisher Site
Abstract
Recently, clinical features of adult‐onset neuronal intranuclear inclusion disease have gradually become characterized by premortem diagnoses based on eosinophilic, ubiquitin‐positive intranuclear inclusions demonstrated using skin biopsy specimens. A 65‐year‐old healthy woman with proteinuria was admitted because of cognitive impairment and walking instability. She had frontal lobe dysfunction and sensory ataxia with high‐signal‐intensity lesions in the corticomedullary junction on performing diffusion‐weighted brain magnetic resonance imaging. She was incidentally diagnosed with adult‐onset sporadic neuronal intranuclear inclusion disease based on the presence of intranuclear inclusions in renal biopsy specimens. Proteinuria might be a non‐neuronal symptom of neuronal intranuclear inclusion disease because no other causes for proteinuria were found on renal testing.
Journal
Neurology and Clinical Neuroscience – Wiley
Published: Jan 1, 2018
Keywords: ; ; ;