Outer retinal tubulations in maternally inherited diabetes and deafness (MIDD)-associated macular dystrophy

Graefe's Archive for Clinical and Experimental Ophthalmology

Volumn 251, Issue 9, 2013, Pages 2265-2267

  Raja, Muhammad S ^a   Goldsmith, C ^a   Burton, B J L ^a  

^a JAMES PAGET UNIVERSITY HOSPITALS NHS FOUNDATION TRUST   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

MITOCHONDRIAL DNA;

AGED; AUTOFLUORESCENCE; AUTOFLUORESCENCE IMAGING; B SCAN; CASE REPORT; CAUCASIAN; CLINICAL EVALUATION; CLINICAL FEATURE; DISEASE ASSOCIATION; FEMALE; FUNDUS AUTOFLUORESCENCE; HISTOPATHOLOGY; HUMAN; INFRARED REFLECTANCE NEAR INFRARED AUTOFLUORESCENCE; LETTER; MATERNALLY INHERITED DIABETES AND DEAFNESS; NUCLEOTIDE SEQUENCE; OPTICAL COHERENCE TOMOGRAPHY; OUTER RETINAL TUBULATION; PHOTORECEPTOR; PIGMENT EPITHELIUM; PRIORITY JOURNAL; RETINA DISEASE; RETINA MACULA AGE RELATED DEGENERATION; VISUAL ACUITY;

AGED; DEAFNESS; DIABETES MELLITUS, TYPE 2; DNA, MITOCHONDRIAL; FEMALE; FLUORESCEIN ANGIOGRAPHY; HUMANS; MACULAR DEGENERATION; MULTIMODAL IMAGING; POINT MUTATION; RETINAL PHOTORECEPTOR CELL OUTER SEGMENT; TOMOGRAPHY, OPTICAL COHERENCE; VISUAL ACUITY;

EID: 84885584974     PISSN: 0721832X     EISSN: 1435702X     Source Type: Journal    
DOI: 10.1007/s00417-012-2217-z     Document Type: Letter

References (5)

1. Zweifel SA, Engelbert M, Laud K, Margolis R, Spaide RF, Freund KB (2009) Outer retinal tubulations: a novel optical coherence tomography finding. Arch Ophthalmol 127:1596-1602
2. Gallego-Pinazo R, Marsiglia M, Mrejen S, Yannuzzi L (2012) Outer retinal tubulations in chronic central serous retinopathy. Graefes Arch Clin Exp Ophthalmol Sep 7 [epub ahead of print]. doi: 10.1007/s00417-012-2151-0
3. Strauss DS, Freund KB (2012) Diagnosis of maternally inherited diabetes and deafness (mitochondrial A3243G mutation) based on fundoscopic appearance in an asymptomatic patient. Br J Ophthalmol 96(4):604
4. Michaelides M, Jenkins SA, Bamiou DE, Sweeney MG, Davis MB, Luxol L, Bird AC, Rath PP (2008) Macular dystrophy associated with the A3243G mitochondrial DNA mutation. Distinct retinal and associated features, disease variability, and characterization of asymptomatic family members. Arch Ophthalmol 126(3):320-328
5. Murphy R, Turnbull DM, Walker M, Hattersley AT (2008) Clinical features, diagnosis and management of maternally inherited diabetes and deafness (MIDD) associated with the 3243A>G mitochondrial point mutation. Diabet Med 25(4):383-399