Cases with familial diffuse leukoencephalopathy

Author:

Mitsuyama Yoshio1,Inoue Teruhiko1,Hayashi Yoshihito1,Mera Seigo2

Affiliation:

1. Psychogeriatric Center, Daigo Hospital, Mimata

2. Department of Psychiatry, Inoue Hospital, Miyazaki

Publisher

The Kyushu Association of Neuropsychiatry

Subject

General Earth and Planetary Sciences,General Environmental Science

Reference18 articles.

1. 1) Nasu, T.: General pathology of membranous lipodystrophy. In: Yonezawa, T. editor. International symposium on the leukoencepalopathy and allied diseases. Kyoto: The Japanese Society of Neuropathology, Pp.61-78, 1981.

2. 2) Hakola, H. P. A., Jarvi, O. H., Sourander, P.: Osteodysplasia polycystica herediteria combined with sclerosing leukoencepahopathy, a new entity of the dementia praesenilis group. Acta Neurol Scand Suppl, 46:79-80, 1970.

3. 3) 小柳清光,木下通亭:Nasu-Hakola病:ミクログリアと破骨細胞異常による脳白質変性と骨病変.神経内科,89:91-98,2018.

4. 4) Bianchin, M. M., Capella, H. M., Chaves, D. L. et al.: Nasu-Hakola disease (polycystic lipomembraneous osteodysplasia with sclerosing leukoencephalopathy; PLOS): a dementia associated with bone cystic lesions. From clinical to genetic and molecular aspects. Cell Mol Neurobiol, 24:1-24, 2004.

5. 5) Hakola, H. P. A.: Neuropsychiatric and genetic aspects of a new hereditary disease characterized by progressive dementia and liopomembraneous polycystic osteodysplasia. Acta Psychiatr Scand Suppl, 232:1-173, 1972.

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