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Leber plus disease
Atipo-Tsiba, P. W.
  • Atipo-Tsiba, P. W; s.af
Rwanda med. j. (Online) ; 71(3): 26-27, 2013. ilus
Article in English | AIM | ID: biblio-1269610
ABSTRACT

Introduction:

Leber's neuropathy is a rare disease. The ''Leber Plus' is exceptional; is associated with a severe neurological disorder. This presentation was intended to describe a case of Leber Plus.

Methods:

A 45-year-old man consulted our department for bilateral blindness since 15 years

Results:

On both sides there was no light perception; optic atrophy with serious peripapillary vessels sclerosis. There was a flccid paraplegia. The 11 778 mitochondrial DNA mutation was identifid.

Conclusion:

The prevalence of the Leber's neuropathy is probably underestimated in black Africa because of lack of molecular biology laboratory
Subject(s)
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Index: AIM (Africa) Main subject: Paraplegia / Case Reports / Blindness / Optic Atrophy, Hereditary, Leber Type of study: Prognostic study / Risk factors Language: English Journal: Rwanda med. j. (Online) Year: 2013 Type: Article

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Index: AIM (Africa) Main subject: Paraplegia / Case Reports / Blindness / Optic Atrophy, Hereditary, Leber Type of study: Prognostic study / Risk factors Language: English Journal: Rwanda med. j. (Online) Year: 2013 Type: Article