Acute metabolic cataract as a first manifestation of diabetes mellitus in a 12-year-old girl [2]

Diabetologia

Volumn 47, Issue 3, 2004, Pages 592-593

  Suzuki, Y ^a,b,c,d   Atsumi, Y ^a   Matsuoka, K ^a   Nishimaki, ^b   Ohta, S ^b   Taniyama, M ^c   Muramatsu, T ^e  

^a SAISEIKAI CENTRAL HOSPITAL   (Japan)

^b Graduate School of Medicine   (Japan)

^c SHOWA UNIVERSITY FUJIGAOKA HOSPITAL   (Japan)

^d Hoken Dohjin Medical Foundation   (Japan)

^e KEIO UNIVERSITY   (Japan)

Author keywords

3243 mitochondrial tRNA mutation; Juvenile cataract; MELAS; Mitochondrial diabetes; Oxidative stress

Indexed keywords

ANTIDIABETIC AGENT; INSULIN;

CASE REPORT; CATARACT; CATARACT EXTRACTION; DIAGNOSTIC PROCEDURE; FEMALE; GLOBUS PALLIDUS; HUMAN; LETTER; NEUROIMAGING; NON INSULIN DEPENDENT DIABETES MELLITUS; PARESTHESIA; POLYDIPSIA; PRIORITY JOURNAL; REAL TIME POLYMERASE CHAIN REACTION; SCHOOL CHILD;

ADULT; CATARACT; CHILD; DIABETES MELLITUS, TYPE 1; DIABETES MELLITUS, TYPE 2; DIABETIC RETINOPATHY; DNA, MITOCHONDRIAL; FEMALE; GLOBUS PALLIDUS; HUMANS; MAGNETIC RESONANCE IMAGING;

EID: 1842844408     PISSN: 0012186X     EISSN: None     Source Type: Journal    
DOI: 10.1007/s00125-004-1333-7     Document Type: Letter

References (5)

1. Nomiyama T, Tanaka Y, Hattori N et al. (2002) Accumulation of somatic mutation in mitochondrial DNA extracted from peripheral blood cells in diabetic patients. Diabetologia 45:1577-1583
2. Falck A, Laatikainen L (1998) Diabetic cataract in children. Acta Ophthalmol Scand 76:238-240
3. Isashiki Y, Nakagawa M, Ohba N et al. (1998) Retinal manifestations in mitochondrial diseases associated with mitochondrial DNA mutation. Acta Ophthalmol Scand 76:6-13
4. Terauchi A, Tamagawa K, Morimatsu Y et al. (1996) An autopsy case of mitochondrial encephalomyopathy, lactic acidosis and stroke-like episodes (MELAS) with a point mutation of mitochondrial DNA. Brain Dev 18:224-229
5. Yasukawa T, Suzuki T, Ishii N et al. (2001) Wobble modification defect in tRNA disturbs codon-anticodon interaction in a mitochondrial disease. EMBO J 20:4794-4802