Literature DB >> 6870629

Ophthalmoscopic findings in Leber's hereditary optic neuropathy. II. The fundus findings in the affected family members.

E Nikoskelainen, W F Hoyt, K Nummelin.   

Abstract

Eighteen men and four women had Leber's disease. Fundus photographs obtained in three cases showed the following: Peripapillary microangiopathy, present from the beginning, slowly increased during the presymptomatic stage. At the end of the presymptomatic stage, the nerve fiber layer became swollen. During the acute stage, retinal vessels on and around the disc were dilated, tortuous, and telangiectatic. Nerve fiber layer hemorrhages occurred in two eyes. As atrophy appeared first in the papillomacular bundle and then in the remaining retina, the vascular bed involuted, leaving a capillary-poor retina with attenuated arterioles and a pale optic disc. The final degree of atrophy varied. Fifteen of the affected persons were blind with severe optic atrophy, but in seven optic atrophy was only partial, causing less visual handicap. Our results suggest that Leber's disease is primarily an intraocular, not a retrobulbar, optic neuropathy. It should be redesignated as Leber's hereditary neuroretinopathy.

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Mesh:

Year:  1983        PMID: 6870629     DOI: 10.1001/archopht.1983.01040020061011

Source DB:  PubMed          Journal:  Arch Ophthalmol        ISSN: 0003-9950


  25 in total

1.  A variant of Leber hereditary optic neuropathy characterized by recovery of vision and by an unusual mitochondrial genetic etiology.

Authors:  D Mackey; N Howell
Journal:  Am J Hum Genet       Date:  1992-12       Impact factor: 11.025

2.  Genetic heterogeneity and mitochondrial DNA heteroplasmy in Leber's hereditary optic neuropathy.

Authors:  I J Holt; D H Miller; A E Harding
Journal:  J Med Genet       Date:  1989-12       Impact factor: 6.318

3.  Deficiency of thiosulphate sulphurtransferase (rhodanese) in Leber's hereditary optic neuropathy.

Authors:  C J Poole; P R Kind
Journal:  Br Med J (Clin Res Ed)       Date:  1986-05-10

4.  Magnetic resonance imaging in Leber's optic neuropathy.

Authors:  A G Kermode; I F Moseley; B E Kendall; D H Miller; D G MacManus; W I McDonald
Journal:  J Neurol Neurosurg Psychiatry       Date:  1989-05       Impact factor: 10.154

5.  Studies on Leber's optic neuropathy III.

Authors:  A Palan; A Stehouwer; L N Went
Journal:  Doc Ophthalmol       Date:  1989-01       Impact factor: 2.379

6.  Leber's hereditary optic atrophy: further evidence for a defect of cyanide metabolism?

Authors:  T A Berninger; L von Meyer; E Siess; O Schon; F D Goebel
Journal:  Br J Ophthalmol       Date:  1989-04       Impact factor: 4.638

7.  Restriction endonuclease analysis of leukocyte mitochondrial DNA in Leber's optic atrophy.

Authors:  I J Holt; D H Miller; A E Harding
Journal:  J Neurol Neurosurg Psychiatry       Date:  1988-08       Impact factor: 10.154

8.  Foveal pit morphological changes in asymptomatic carriers of the G11778A mutation with Leber's hereditary optic neuropathy.

Authors:  Xin-Ting Liu; Mei-Xiao Shen; Chong Chen; Sheng-Hai Huang; Xi-Ran Zhuang; Qing-Kai Ma; Qi Chen; Fan Lu; Yi-Min Yuan
Journal:  Int J Ophthalmol       Date:  2020-05-18       Impact factor: 1.779

Review 9.  Leber's hereditary optic neuropathy: the clinical relevance of different mitochondrial DNA mutations.

Authors:  P Riordan-Eva; A E Harding
Journal:  J Med Genet       Date:  1995-02       Impact factor: 6.318

Review 10.  A review of primary hereditary optic neuropathies.

Authors:  M Votruba; S Aijaz; A T Moore
Journal:  J Inherit Metab Dis       Date:  2003       Impact factor: 4.982

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