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ISSN: 2572-4983

Neonatal and Pediatric Medicine
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  • Case Report   
  • Neonat Pediatr Med 2016, Vol 2(1): S1009
  • DOI: 10.4172/2572-4983.1000S1009

Leber's (Plus?) Hereditary Optic Neuropathy: A Case Report

Arife CA1*, Cansu S2 and Ufuk E1
1Department of Neurology, Istanbul Education and Research Hospital, , Istanbul, Turkey
2Istanbul Education and Research Hospital, , Istanbul, Turkey
*Corresponding Author : Arife CA, Department of Neurology, Istanbul Education and Research Hospital, Istanbul, Turkey, Tel: 905338141817, Email: cimenatalar@yahoo.com.tr

Received Date: Nov 16, 2016 / Accepted Date: Dec 03, 2016 / Published Date: Dec 10, 2016

Abstract

Leber's hereditary optic neuropathy (LHON)-plus is a maternally inherited genetic disorder of young males and characterized by severe progressive vision loss with other neurological and systemic symptoms. Here we present a young male with subacute progressive vision loss and Parkinsonism symptoms like right arm rigidity and endocrine abnormalities like hypoparathyroidism as a probable LHON-plus case.

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Citation: Arife CA, Cansu S, Ufuk E (2016) Leber’s (Plus?) Hereditary Optic Neuropathy: A Case Report. Neonat Pediatr Med 2: S1009. Doi: 10.4172/2572-4983.1000S1009

Copyright: © 2016 Arife CA, et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

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