Late onset cerebello-pontomesencephalic degeneration

Two siblings are presented with late onset, rapidly progressive truncal ataxia, paralysis of down-gaze and loss of up-gaze saccades in association with other oculomotor dysfunctions as well as dementia. Electron microscopic muscle studies revealed abnormal distribution and form of the mitochondria,...

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Veröffentlicht in:	Journal of the neurological sciences 1989-11, Vol.93 (2), p.323-331
Hauptverfasser:	Al-Din, Amir S.Najim, Al-Zuhair, Ali G.H., Al-Salem, Mahmoud K., Al-Nassar, Khalid Eid, Rudwan, Mohammed A., Khafaja, Salah, Hamawi, Tawfiq
Format:	Artikel
Sprache:	eng
Schlagworte:	Brain Diseases - genetics Brain Diseases - pathology Brain Diseases - physiopathology Cerebellar degeneration Cerebellopontine Angle - physiopathology Cerebellopontine Angle - ultrastructure Dementia Dementia - etiology Down-gaze paralysis Humans Late onset Male Middle Aged Mitochondria, Muscle - ultrastructure Pedigree Vertical gaze paralysis
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