Hereditary renal and retinal dysplasia--the Senior-Loken syndrome.
作者信息
Bell A H, McKiernen P J, Savage J M, Reid M M
出版信息
Ulster Med J. 1987 Oct;56(2):160-2.
Abstract
摘要
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Hereditary renal and retinal dysplasia--the Senior-Loken syndrome.遗传性肾视网膜发育不良——Senior-Loken综合征
Ulster Med J. 1987 Oct;56(2):160-2.
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[Hereditary peripheral chorioretinal dysplasia].[遗传性周边脉络膜视网膜发育异常]
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Nephronophthisis and retinal degeneration in tmem218-/- mice: a novel mouse model for Senior-Løken syndrome?Tmem218基因敲除小鼠中的肾单位肾痨和视网膜变性：一种用于Senior-Løken综合征的新型小鼠模型？
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[Electroretinography in nephronophthisis. Role of the Senior-Loken syndrome].[肾单位肾痨的视网膜电图。Senior-Loken综合征的作用]
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Senior-Loken syndrome. Case reports of two siblings and association with sensorineural deafness.Senior-Loken综合征。两例同胞病例报告及其与感音神经性耳聋的关联。
Br J Ophthalmol. 1992 Mar;76(3):171-2. doi: 10.1136/bjo.76.3.171.
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Gyrate atrophy of the choroid and retina.脉络膜和视网膜的回旋状萎缩
Prog Clin Biol Res. 1982;82:123-34.
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[Senior-Löken retino-tubular degeneration].[Senior-Löken视网膜-肾小管变性]
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引用本文的文献
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The Senior-Loken syndrome: Two cases from the State of Qatar.Senior-Loken综合征：卡塔尔的两例病例。
J Clin Diagn Res. 2012 Oct;6(8):1411-3. doi: 10.7860/JCDR/2012/4131.2372.
本文引用的文献
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Juvenile familial nephropathy with tapetoretinal degeneration. A new oculorenal dystrophy.伴有视网膜色素变性的青少年家族性肾病。一种新的眼肾营养不良症。
Am J Ophthalmol. 1961 Nov;52:625-33. doi: 10.1016/0002-9394(61)90147-7.
2
Hereditary renal dysplasia and blindness.遗传性肾发育不全与失明。
Acta Paediatr (Stockh). 1961 Mar;50:177-84. doi: 10.1111/j.1651-2227.1961.tb08037.x.
3
Absence of the cerebellar granular layer, mental retardation, tapetoretinal degeneration and progressive glomerulopathy: an autosomal recessive oculo-renal-cerebellar syndrome.小脑颗粒层缺失、智力发育迟缓、视网膜色素变性和进行性肾小球病：一种常染色体隐性眼-肾-小脑综合征。
Am J Med Genet. 1982 Apr;11(4):383-95. doi: 10.1002/ajmg.1320110403.
4
Leber's congenital amaurosis associated with familial juvenile nephronophthisis and cone-shaped epiphyses of the hands (the Saldino-Mainzer syndrome).与家族性青少年肾单位肾痨及手部锥形骨骺相关的莱伯先天性黑矇（萨尔迪诺－梅恩泽尔综合征）
Am J Ophthalmol. 1984 Feb;97(2):233-9. doi: 10.1016/s0002-9394(14)76095-7.
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