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Acta clinica Croatica, Vol. 41 No. 4 Suppl - OPHTHALMOL, 2002.

Conference paper

Leber's Hereditary Optic Neuropathy. A Case Report

Jelena Petrinović-Dorešić
Ljerka Hene-Petrinović
Biljana Kuzmanović

Full text: english pdf 135 Kb

page 81-85

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Abstract

LHON is characterized by bilateral asynchronous visual loss in young adults. This type of neuropathy is related to mitochondrial DNA mutation and therefore is maternally inherited. Males are predominantly affected but they do not transmit the disease to their offspring. Clinical picture - although characteristic - is not impressive. At the beginning of the disease, there is a large discrepancy between the symptoms and signs. In contrast to marked central visual loss, the only visible sign is retinal teleangiectatic microangiopathy in the peripapillary region. Fluorescein angiography shows intact capillary network without leakage disproving its inflammatory nature.

Keywords

Hereditary optic atrophy; mitochondrial DNA mutation

Hrčak ID:

15008

URI

https://hrcak.srce.hr/15008

Publication date:

1.11.2002.

Article data in other languages: croatian

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