Mitochondrial Diseases in Pediatric Ophthalmology

Journal of AAPOS

Volumn 1, Issue 2, 1997, Pages 115-122

  Phillips, Paul H ^a   Newman, Nancy T ^a,b  

^a EMORY UNIVERSITY SCHOOL OF MEDICINE   (United States)

^b EMORY EYE CENTER   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

CHILD; EYE DISEASE; GENETICS; HUMAN; MITOCHONDRIAL MYOPATHY; REVIEW;

CHILD; EYE DISEASES; HUMANS; MITOCHONDRIAL MYOPATHIES;

EID: 0031150466     PISSN: 10918531     EISSN: None     Source Type: Journal    
DOI: 10.1016/S1091-8531(97)90010-0     Document Type: Article

References (14)

1. Newman NJ. Mitochondrial disease and the eye. Ophthalmol Clin North Am 1992;5:405-24.
2. Newman NJ, Lott MT, Wallace DC. The clinical characteristics of pedigrees of Leber's hereditary optic neuropathy with the 11778 mutation. Am J Ophthalmol 1991;111:750-62.
3. Riordan-Eva P, Sanders MD, Govan GG, Sweeney MG, Da Costa J, Harding AE. The clinical features of Leber's hereditary optic neuropathy defined by the presence of a pathogenic mitochondrial DNA mutation. Brain 1995;118:319-37.
4. Newman NJ. Neuro-ophthalmology and systemic disease. Part I. An annual review (1994). J Neuroophthalmol 1995;15:109-21.
5. Johns DR, Smith KH, Miller NR. Leber's hereditary optic neuropathy: clinical manifestations of the 3460 mutation. Arch Ophthalmol 1992;110:1577-81.
6. Johns DR, Heher KL, Miller NR, Smith KH. Leber's hereditary optic neuropathy: clinical manifestations of the 14484 mutation. Arch Ophthalmol 1993;111:495-8.
7. Newman NJ. Leber's hereditary optic neuropathy: new genetic considerations. Arch Neurol 1993;50:540-8.
8. Weiner NC, Newman NJ, Lessell S, Johns DR, Lott MT, Wallace DC. Atypical Leber's hereditary optic neuropathy with molecular confirmation. Arch Neurol 1993;50:470-3.
9. Wallace DC, Singh D, Lott MT, et al. Mitochondrial DNA mutation associated with Leber's hereditary optic neuropathy. Science 1988;242:1422.
10. Swartz N, Savino PJ. Is all nondefinable optic atrophy Leber's hereditary optic neuropathy? Surv Ophthalmol 1994;39:146-50.
11. Newman NJ. Neuro-ophthalmology and systemic disease: an annual review (1993). J Neuroophthalmol 1994;14:105-17.
12. Fang W, Huang CC, Lee CC, Cheng SY, Pang CY, Wei YH. Ophthalmologic manifestations in MELAS syndrome. Arch Neurol 1993;50:977-80.
13. Ortiz RG, Newman NJ, Shoffner JM, Kaufman AE, Koontz DA, Wallace DC. Variable retinal and neurologic manifestations in patients harboring the mitochondrial DNA 8993 mutation. Arch Ophthalmol 1993;111:1525-30.
14. Massin P, Guillausseau PJ, Vialettes B, et al. Macular pattern dystrophy associated with a mutation of mitochondrial DNA. Am J Ophthalmol 1995;120:247-8.