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色素失禁症（布洛赫-苏尔茨贝格综合征）与视网膜病变。

Incontinentia pigmenti (Bloch-Sulzberger syndrome) and retinal changes.

作者信息

François J

出版信息

Br J Ophthalmol. 1984 Jan;68(1):19-25. doi: 10.1136/bjo.68.1.19.

DOI:10.1136/bjo.68.1.19
PMID:6689930
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1040231/
Abstract

Incontinentia pigmenti is associated with various anomalies in 80% of cases. Among the most important are the ocular abnormalities and more particularly a retrolental mass with detachment of a dysplastic retina. At the basis of this manifestation are retinal vascular changes, characterised at first by ectatic tortuous veins and arteriovenous anastomoses as well as by aneurysmal-like dilatations.

摘要

色素失禁症在80%的病例中与各种异常有关。其中最重要的是眼部异常，尤其是晶状体后肿块伴发育异常视网膜脱离。这种表现的基础是视网膜血管变化，最初表现为扩张迂曲的静脉、动静脉吻合以及动脉瘤样扩张。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d557/1040231/c177569f706b/brjopthal00145-0040-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d557/1040231/e3684bef5774/brjopthal00145-0036-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d557/1040231/427eeaf2fb97/brjopthal00145-0036-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d557/1040231/6e3173fda767/brjopthal00145-0039-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d557/1040231/df5a7ad2546b/brjopthal00145-0039-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d557/1040231/1a9d968cd388/brjopthal00145-0039-c.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d557/1040231/be235541a6cd/brjopthal00145-0040-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d557/1040231/c177569f706b/brjopthal00145-0040-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d557/1040231/e3684bef5774/brjopthal00145-0036-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d557/1040231/427eeaf2fb97/brjopthal00145-0036-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d557/1040231/6e3173fda767/brjopthal00145-0039-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d557/1040231/df5a7ad2546b/brjopthal00145-0039-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d557/1040231/1a9d968cd388/brjopthal00145-0039-c.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d557/1040231/be235541a6cd/brjopthal00145-0040-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d557/1040231/c177569f706b/brjopthal00145-0040-b.jpg

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Incontinentia pigmenti (Bloch-Sulzberger syndrome) and retinal changes.色素失禁症（布洛赫-苏尔茨贝格综合征）与视网膜病变。
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本文引用的文献

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On the pathogenesis of incontinentia pigmenti, with observations on an associated eye disturbance resembling retrolental fibroplasia.
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The Bloch-Sulzberger syndrome (incontinentia pigmenti).布洛赫-苏尔茨贝格综合征（色素失禁症）。
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Incontinentia pigmenti; a report of five cases and review of the literature.色素失禁症；五例报告及文献复习
Indian J Ophthalmol. 2019 Jun;67(6):940-942. doi: 10.4103/ijo.IJO_760_18.
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Incontinentia pigmenti.色素失禁症
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Persistent Fetal Vasculature and Severe Protein C Deficiency.持续性胎儿血管系统与严重蛋白C缺乏症
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Novel corneal features in two males with incontinentia pigmenti.两名色素失禁症男性患者的新型角膜特征。
Br J Ophthalmol. 2003 May;87(5):554-6. doi: 10.1136/bjo.87.5.554.
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Incontinentia pigmenti (Bloch-Sulzberger syndrome).色素失禁症（布洛赫-苏尔茨贝格综合征）。
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The blinding mechanisms of incontinentia pigmenti.色素失禁症的致盲机制。
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Incontinentia pigmenti: the development of pseudoglioma.色素失禁症：假性胶质瘤的发展。
Br J Ophthalmol. 1988 Jun;72(6):452-5. doi: 10.1136/bjo.72.6.452.
10
Mapping the gene for X-linked cataracts and microcornea with facial, dental, and skeletal features to Xp22: an appraisal of the Nance-Horan syndrome.将伴有面部、牙齿和骨骼特征的X连锁白内障和小角膜基因定位到Xp22：对南斯-霍兰综合征的评估
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Incontinentia pigment: a report of three cases in one family.色素失禁症：一家系三例报告
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Ocular changes in the Bloch-Sulzberger syndrome (Incontinentia pigmenti).布洛赫-苏尔茨贝格综合征（色素失禁症）的眼部变化。
Br J Ophthalmol. 1955 May;39(5):276-82. doi: 10.1136/bjo.39.5.276.
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[INCONTINENTIA PIGMENTI. REPORT OF NINE CASES IN ONE FAMILY AND ON ONE NECROSPY INVESTIGATION].[色素失禁症。一个家族中九例病例报告及一例尸检研究]
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[INCONTINENTIA PIGMENT WITH OCULAR INVOLVEMENT].[伴有眼部受累的色素失禁症]
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Fundus changes in incontinentia pigmenti (Bloch-Sulzberger syndrome).色素失禁症（布洛赫-苏尔茨贝格综合征）的眼底改变。
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