A Nation-Wide Survey for Neurologic and Hepato-Neurologic Type of Wilson Disease: Clinical Features and Hepatic Copper Content.
-
- Shimizu Norikazu
- Second Department of Pediatrics, Toho University School of Medicine
-
- Suzuki Mariko
- Second Department of Pediatrics, Toho University School of Medicine
-
- Yamaguchi Yukitoshi
- Second Department of Pediatrics, Toho University School of Medicine
-
- Aoki Tsugutoshi
- Second Department of Pediatrics, Toho University School of Medicine
-
- Matsuda Ichiro
- Department of Pediatrics, Kumamoto University
-
- Arima Masataka
- National Center Hospital for Mental, Nervous, and Muscular Disorders, National Center of Neurology and Psychiatry
Bibliographic Information
- Other Title
-
- 全国調査からみた神経型・肝神経型Wilson病の臨床像および肝銅含量に関する検討
Search this article
Description
A nation-wide survey for Wilson disease was performed from 1990 to 1991. We studied clinical features and copper content in liver for the neurologic and hepato-neurologic types. A questionnaire was sent to more than five thousand hospitals in Japan. Thirty-three percent of physicians completed the questionnaire. Four hundred and twenty-five cases were studied for the onset age, primary symptoms, prognosis and hepatic copper content. The onset age of neurologic and hepato- neurologic type of Wilson disease was usually 6 years or older. The most common initial symptom was dysarthria. Gait disturbance, flapping tremor and Kayser-Fleischer rings were also very common symptoms. We conclude that in patients with disarthria and/or extra pyramidal symptoms over 6 years of age, Wilson disease should be considered. The prognosis quod vitam of patients with neurologic and hepato-neurologic Wilson disease is not always fatal. However, many patients required prolonged treatment at either a hospital, sanatorium or at home due to irreversibility of their severe neurological defects. This result shows that early detection is the most important factor for a promising prognosis. Copper content in liver was examined for each type of Wilson disease. Neurologic type of Wilson disease had the highest copper content, followed by hepato-neurologic type. Hepatic type had the lowest copper level out of these three forms of the disease. The mechanism of onset for each type of Wilson disease should be studied using these results.
Journal
-
- NO TO HATATSU
-
NO TO HATATSU 28 (5), 391-397, 1996
THE JAPANESE SOCIETY OF CHILD NEUROLOGY
- Tweet
Keywords
Details 詳細情報について
-
- CRID
- 1390001204554750592
-
- NII Article ID
- 130004068146
- 10005658038
-
- NII Book ID
- AN0020232X
-
- ISSN
- 18847668
- 00290831
-
- PubMed
- 8831241
-
- Text Lang
- ja
-
- Data Source
-
- JaLC
- PubMed
- CiNii Articles
-
- Abstract License Flag
- Disallowed