NTCC® NA10624 LCL DNA-BioVector NTCC典型培养物保藏中心Coriell NA10624
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- 货 号:NTCC®-Coriell NA10624
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Name:NTCC® NA10624 LCL DNACategory分类:DNACat#货号:NTCC®-Coriell NA10624Size/Quantity数量: 1 VialBiosafety Level生物安全级别:1Shipping Info运输方式: RTStorage储存方式: 4CSpecies物种来源: Age年龄: 50 YRGender性别: MaleDescription描述: CONGENITAL OPTIC ATROPHY, TYPE UNKNOWNRemarks: Clinically affected; onset in mid-teens (age 17 years); rapid onset of visual loss in teens, starting with slightly blurry vision then progressive deterioration of visual acuity within a span of months; underwent exploratory craniotomy and optic nerve sheath decompression for scar tissue on the optic nerve; very slow progression, if any, since mid-teens; visual acuity noted to be 20/400 in either eye (with correction); Ishihara contrast plate testing: no plates were identifiable by donor subject; Farnsworth Dichotomous Test for color blindness revealed primarily a tritan deficiency in the right eye, although mixed abnormalities were present. In the left eye deutan and tritan abnormalities with a mixed deficit were identified; optic atrophy of 3-4+ was present with marked "pipes-on-the-ground" appearance of the retinal vessels due to retinal nerve fiber layer atrophy; ERG showed photopic O.D. and O.S. having subnormal amplitudes with normal implicit times; scotopic O.S. has subnormal amplitudes and borderline normal implicit times, which suggests congenital photoreceptor loss with O.S. worse than O.D.; Goldman visual field demonstrated enlargement of blindspot superiorly in right eye, and a superior central scotoma with a sharp linear margin and the horizontal meridian; enlargement of the blind spot in the left eye with a cecocentral pattern involving area of central fixation, a smaller more dense area was present between 10 and 20 degrees superiorly; mitochondrial DNA retains the Sfa NI restriction site, indicating subject is negative for Leber's optic atrophy; see GM10625 (fibro); affected brother is GM03857 (lymph) and GM03858 (fibro).Alternate IDs其他编号: Cell Type细胞类型:
LCLSource组织来源: LCLGene: Disease疾病类型: Mutations突变: Karyotypes核型: Cytogenetics: Mutation description突变描述: Origin: Transformants: Alias别名: Images图片:References参考文献:Supplier供应商:BioVector质粒载体菌株细胞蛋白抗体基因保藏中心
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