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1 атрофия зрительного нерва Лебера
Leber's optic atrophy, Leber's diseaseБольшой русско-английский медицинский словарь > атрофия зрительного нерва Лебера
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2 болезнь Лебера
Medicine: Leber's disease, Leber's optic atrophy (синдром), Leber hereditary optic atrophy, Leber’s acute optic neuropathy, Leber's atrophy, Leber's hereditary optic neuropathy, hereditary optic neuroretinopathy, Leber's optic neuropathy -
3 наследственная оптическая нейропатия Лебера
1) General subject: Leber's disease (наследственная атрофия зрительных нервов, обусловленная нарушением фосфорилирующей функции митохондрий вследствие генетических дефектов митохондриальной ДНК,)2) Medicine: Leber hereditary optic atrophy, Leber’s acute optic neuropathy, Leber's atrophy, Leber's hereditary optic neuropathy, hereditary optic neuroretinopathy, Leber's optic neuropathyУниверсальный русско-английский словарь > наследственная оптическая нейропатия Лебера
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4 синдром Лебера
Medicine: Leber hereditary optic atrophy, Leber’s acute optic neuropathy, Leber's atrophy, Leber's disease, Leber's hereditary optic neuropathy, hereditary optic neuroretinopathy, Leber's optic neuropathy -
5 наследственная атрофия зрительных нервов
Medicine: Leber's disease, Leber's optic atrophyУниверсальный русско-английский словарь > наследственная атрофия зрительных нервов
См. также в других словарях:
Leber’s disease — congenital atrophy of the optic nerve … Eponyms, nicknames, and geographical games
Leber's hereditary optic neuropathy — Classification and external resources ICD 10 H47.2 ICD 9 377.16 … Wikipedia
Leber's congenital amaurosis — Classification and external resources ICD 10 H53.0 ICD 9 362.76 … Wikipedia
Leber hereditary optic neuropathy — Leber optic neuropathy a rare hereditary disorder due to mutation in any of multiple genes encoded by the mitochondrial genome, showing variable penetrance, and in Caucasians preferentially expressed in males. It is characterized by degeneration… … Medical dictionary
Leber disease — Leber hereditary optic neuropathy … Medical dictionary
Leber's Congenital Amaurosis (LCA) and hallucinations — The eponym Leber s congenital amaurosis refers to the German ophthalmologist Theodor Karl Gustav von Leber (1840 1917), who was the first to describe the concomitant condition in 1869. LCA is considered a type of amaurosis, due to an autosomal … Dictionary of Hallucinations
Leber's congenital amaurosis — a hereditary disease (inherited as an autosomal recessive inherited condition) causing severe visual loss in infants. The back of the eye appears to be normal when examined with an ophthalmoscope, but marked abnormalities are found on the ERG… … Medical dictionary
Leber's congenital amaurosis — a hereditary disease (inherited as an autosomal recessive condition) causing severe visual loss in infants. The fundus usually appears to be normal when examined with an ophthalmoscope, but marked abnormalities are found on the ERG (see… … The new mediacal dictionary
Disease, mitochondrial — Mutations (changes) in the mitochondrial chromosome are responsible for a number of disorders including, for example: An eye disease called Leber s hereditary optic atrophy; A type of epilepsy called MERRF which stands for Myoclonus Epilepsy with … Medical dictionary
enfermedad de Leber — Eng. Leber s disease 1. Ver Amaurosis congénita de Leber. 2. Ver Aneurismas miliares de Leber … Diccionario de oftalmología
Polyzystische Leber — Klassifikation nach ICD 10 K44.6 Zystenleber … Deutsch Wikipedia