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J Clin Neuroophthalmol ; 6(2): 76-81, 1986 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-2942573

RESUMO

The case of a patient with Charcot-Marie-Tooth disease who developed the acute fundus findings of Leber's optic neuropathy is described. Previous reports have proposed a genetic interrelationship between the two diseases. This relationship has been speculative, however, because the acute fundus findings of Leber's have never been observed in a case of Charcot-Marie-Tooth disease. This case adds support for a suggested genetic relationship between the two diseases. It is also possible that the optic atrophy previously described in Charcot-Marie-Tooth may represent the late findings of Leber's optic neuropathy.


Assuntos
Doença de Charcot-Marie-Tooth/complicações , Atrofia Muscular/complicações , Atrofia Óptica/genética , Doença de Charcot-Marie-Tooth/genética , Angiofluoresceinografia , Fundo de Olho , Humanos , Masculino , Pessoa de Meia-Idade , Atrofia Óptica/complicações , Escotoma/genética , Síndrome
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