-transparent.png){kind=logo}
Clinical-neurological, electrocephalographic, ophthalmological and genetic observations of a family with related persons with Leber's optic atrophy is described. 6 male subjects of the altogether ca. 100 members of the family tree stretching over 4 generations were manifestly affected relatives - that is possible carriers, an unusually large number of EEG's were abnormal, and, less often, colour vision disturbances were seen. The results suggest that Leber's optic atrophy is a hereditary neuro-ophthalmological systemic condition, whose most striking symptom is the optic atrophy. The genetic factors of the condition are also discussed.
Related Publications
A Müller-Jensen, and
W Bushart, and
J Steidinger, and
M Funk, and
K A Hellner
January 1980,
Nippon Ganka Gakkai zasshi,
A Müller-Jensen, and
W Bushart, and
J Steidinger, and
M Funk, and
K A Hellner
September 1975,
Klinische Monatsblatter fur Augenheilkunde,
A Müller-Jensen, and
W Bushart, and
J Steidinger, and
M Funk, and
K A Hellner
August 1971,
The Medical journal of Australia,
A Müller-Jensen, and
W Bushart, and
J Steidinger, and
M Funk, and
K A Hellner
December 1990,
Occupational health; a journal for occupational health nurses,
A Müller-Jensen, and
W Bushart, and
J Steidinger, and
M Funk, and
K A Hellner
July 1980,
Indian journal of ophthalmology,
A Müller-Jensen, and
W Bushart, and
J Steidinger, and
M Funk, and
K A Hellner
October 1990,
Klinika oczna,
A Müller-Jensen, and
W Bushart, and
J Steidinger, and
M Funk, and
K A Hellner
May 1977,
Ceskoslovenska oftalmologie,
A Müller-Jensen, and
W Bushart, and
J Steidinger, and
M Funk, and
K A Hellner
September 1989,
Ophthalmic paediatrics and genetics,
A Müller-Jensen, and
W Bushart, and
J Steidinger, and
M Funk, and
K A Hellner
January 1984,
Transactions of the Ophthalmological Society of New Zealand,
A Müller-Jensen, and
W Bushart, and
J Steidinger, and
M Funk, and
K A Hellner
January 1967,
Suomen laakarilehti. Finlands lakartidning,
