Optic Atrophy and Juvenile Diabetes Mellitus with Familial Occurrence

2009 ◽  
Vol 182 (4) ◽  
pp. 419-425 ◽  
Author(s):  
Gunne Rorsman ◽  
Nils Söderström
1976 ◽  
Vol 89 (4) ◽  
pp. 565-570 ◽  
Author(s):  
Tania Gunn ◽  
Robert Bortolussi ◽  
John M. Little ◽  
Frederick Andermann ◽  
F. Clarke Fraser ◽  
...  

1974 ◽  
Vol 23 (S1) ◽  
pp. 187-189 ◽  
Author(s):  
Jean-Real Brunette ◽  
John M. Little

Since the late thirties a syndrome has been progressively completing its description. It consists essentially in juvenile diabetes mellitus, diabetes insipidus, neurosensory hearing loss and optic atrophy. Neurosensory hearing loss, neurogenic bladder, autonomic dysfunction and hyperalanineuria have been added. The syndrome is generally familial.Electrophysiologic and psychophysiological retinal studies have been done in these cases. Profound electrophysiological disturbance has been described. Cases under actual evaluation are presented. Physiopathologic processes remain a problem. The nature of the retinal affection is also open for discussion.


1970 ◽  
Vol 65 (1) ◽  
pp. 95-102 ◽  
Author(s):  
D. G. Ikkos ◽  
G. R. Fraser ◽  
E. Matsouki-Gavra ◽  
M. Petrochilos

ABSTRACT A family is described showing the association of juvenile diabetes mellitus, optic atrophy, and mild perceptive deafness inherited in an autosomal recessive manner. It is pointed out that concomitant diabetes insipidus has predominantly involved females suffering from this association.


Diabetes ◽  
1976 ◽  
Vol 25 (5) ◽  
pp. 420-427 ◽  
Author(s):  
F. M. Bomback ◽  
S. Nakagawa ◽  
S. Kumin ◽  
H. M. Nitowsky

1971 ◽  
Vol 10 (7) ◽  
pp. 385-391
Author(s):  
Joseph B. Warshaw ◽  
Melvin Levine ◽  
Vera Hyman ◽  
John D. Crawford

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