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Familial Raynaud's phenomenon and localized scleroderma associated with essential telangiectasia and cytogenetic abnormalities.

作者信息

Bunker C B, Atherton D, Gray O P, Tsioupra K, Delhanty J D, Dowd P M

机构信息

Department of Dermatology, University College and Middlesex School of Medicine, London.

出版信息

J R Soc Med. 1990 Aug;83(8):531-2. doi: 10.1177/014107689008300821.

DOI:10.1177/014107689008300821
PMID:2231586
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1292786/
Abstract
摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5755/1292786/3190f34be7e2/jrsocmed00133-0064-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5755/1292786/2355ce9e2e08/jrsocmed00133-0063-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5755/1292786/3190f34be7e2/jrsocmed00133-0064-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5755/1292786/2355ce9e2e08/jrsocmed00133-0063-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5755/1292786/3190f34be7e2/jrsocmed00133-0064-a.jpg

相似文献

1
Familial Raynaud's phenomenon and localized scleroderma associated with essential telangiectasia and cytogenetic abnormalities.家族性雷诺现象与局限性硬皮病,伴有原发性毛细血管扩张和细胞遗传学异常。
J R Soc Med. 1990 Aug;83(8):531-2. doi: 10.1177/014107689008300821.
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[Subcutaneous calcinosis, Raynaud's phenomenon, sclerodactyly and telangiectasia (CRST syndrome): an association of interest in hepatology (author's transl)].
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[Primary biliary cirrhosis associated with CRST syndrome (calcinosis, Raynaud's phenomenon, sclerodactyly and telangiectasia). Effect of cytostatic therapy in a case of our observation].
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[Calcinosis-Raynaud's disease-sclerodactylia-telangiectasis syndrome].[钙质沉着-雷诺病-指硬皮病-毛细血管扩张综合征]
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Primary biliary cirrhosis with scleroderma, Raynaud's phenomenon and telangiectasia. New syndrome.
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MULTIPLE TELANGIECTASIA, RAYNAUD'S PHENOMENON, SCLERODACTYLY, AND SUBCUTANIOUS CALCINOSIS: A SYNDROME MIMICKING HEREDITARY HEMORRHAGIC TELANGIECTASIA.多发性毛细血管扩张、雷诺现象、指(趾)硬皮病和皮下钙质沉着:一种酷似遗传性出血性毛细血管扩张症的综合征。
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Telangiectasia in Raynaud's disease.雷诺病中的毛细血管扩张。
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[The CRST syndrome and nodular regenerative hyperplasia of the liver. A case].[CRST综合征与肝脏结节性再生性增生。1例病例]
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引用本文的文献

1
Familial localized scleroderma with paediatric onset: a review.儿童期起病的家族性局限性硬皮病:综述
Postepy Dermatol Alergol. 2021 Apr;38(2):193-197. doi: 10.5114/ada.2021.106195. Epub 2021 May 22.

本文引用的文献

1
Chromosome breakage and sister chromatid exchange frequencies in scleroderma.硬皮病中的染色体断裂和姐妹染色单体交换频率
Arthritis Rheum. 1981 Nov;24(11):1409-13. doi: 10.1002/art.1780241112.
2
Systemic scleroderma. Clinical and pathophysiologic aspects.
J Am Acad Dermatol. 1988 Mar;18(3):457-81. doi: 10.1016/s0190-9622(88)70070-5.
3
Localized scleroderma.
Arch Dermatol. 1975 Jan;111(1):98-100.
4
Systemic scleroderma in mother and daughter.
母女患系统性硬化症。
Arch Dermatol. 1977 Mar;113(3):378-9. doi: 10.1001/archderm.1977.01640030124033.
5
Sister chromatid exchange.姐妹染色单体交换
Annu Rev Genet. 1977;11:183-201. doi: 10.1146/annurev.ge.11.120177.001151.