Volume 36, Issue 3 pp. 441-443
Brief Communications
Full Access

Decreased cerebrospinal fluid levels of β-endorphin in Japanese patients with Joseph disease

Dr. Toyojiro Matsuishi MD

Corresponding Author

Dr. Toyojiro Matsuishi MD

Department of Pediatrics and Child Health, Kurume University School of Medicine Fukuoka, Japan

Department of Pediatrics and Child Health, Kurume University School of Medicine, 67 Asahimachi, Kurume City, Japan 830Search for more papers by this author
Tetsuo Sakai MD

Tetsuo Sakai MD

Department of Neurology, National Ckikugo Hospital, Fukuoka, Japan

Search for more papers by this author
Shinichiro Nagamitsu MD

Shinichiro Nagamitsu MD

Department of Pediatrics and Child Health, Kurume University School of Medicine Fukuoka, Japan

Search for more papers by this author
Hironori Komori MD

Hironori Komori MD

Department of Pediatrics and Child Health, Kurume University School of Medicine Fukuoka, Japan

Search for more papers by this author
Hiroshi Iwashita MD

Hiroshi Iwashita MD

Department of Neurology, National Ckikugo Hospital, Fukuoka, Japan

Search for more papers by this author
Hiroshisa Kato MD

Hiroshisa Kato MD

Department of Pediatrics and Child Health, Kurume University School of Medicine Fukuoka, Japan

Search for more papers by this author
First published: September 1994
Citations: 1

Abstract

We measured the cerebrospinal fluid (CSF) levels of β-endorphin in 7 Japanese patients with Joseph disease and compared them with control values. The 7 patients included 4 with type I and 3 with type II disease; their mean age was 45.7 ± 12.09 years. Diseased controls were matched in age to the patients studied. In these patients, CSF β-endorphin level was significantly lower than in the controls (40% of normal values). An alteration in CSF β-endorphin level may explain some of the neurological impairment found in Joseph disease.

The full text of this article hosted at iucr.org is unavailable due to technical difficulties.

click me