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NEUROLOGY 1985;35:735
© 1985 American Academy of Neurology

Infantile neuroaxonal dystrophy

Perinatal onset with symptoms of diencephalic syndrome

Kanji Nagashima, MD, Shigeyoshi Suzuki, MD, Emiko Ichikawa, MD, Satoshi Uchida, MD, Tetuo Honma, MD, Takayoshi Kuroume, MD, Junko Hirato, MD, Akira Ogawa, MD and Yoichi Ishida, MD

Department of Pediatrics and The First Department of Pathology, Gunma University School of Medicine, Maebashi, Gunma, Japan.

In a neonatal case of infantile neuroaxonal dystrophy, there was emaciation, nystagmus, and endocrinologic disorder suggesting the diencephalic syndrome. At autopsy, spheroid bodies were widely disseminated, particularly in the hypothalamus, inhndibulum, and neurohypophysis. The pathologic process may have started in utero.

Address correspondence and reprint requests to Dr. Nagashima, Department of Pediatrics, Gunma University School of Medicine, 3–39–22 Showamachi, Maebashi-shi, Gunma-ken, Japan.

Accepted for publication September 5, 1984.




This article has been cited by other articles:


Home page
 J Child NeurolHome page
G. Chow and C. J. H. Padfield
A Case of Infantile Neuroaxonal Dystrophy--Connatal Seitelberger Disease
J Child Neurol, April 1, 2008; 23(4): 418 - 420.
[Abstract] [PDF]


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