Incomplete Wolfram syndrome: clinical and electrophysiologic study of two familial cases
Wolfram, or DIDMOAD, syndrome is a genetic disorder characterized by diabetes insipidus, diabetes mellitus, optic atrophy and deafness. We studied a family in which only diabetes mellitus and primary optic atrophy were present in three female siblings. Two of these patients, fraternal twins, were su...
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Veröffentlicht in: | Graefe's archive for clinical and experimental ophthalmology 1989, Vol.227 (2), p.131-135 |
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Sprache: | eng |
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