Do the telangiectases of hereditary hemorrhagic telangiectasia and the calcinosis, Raynaud's disease, sclerodactyly, telangiectasia variant of scleroderma have a common etiology?

被引：2

作者：

Braverman, Irwin M. ^{[1
]}

机构：

[1] Yale Univ, Sch Med, Dept Dermatol, New Haven, CT 06510 USA

来源：

DERMATOLOGY | 2006年 / 213卷 / 02期

关键词：

D O I：

10.1159/000093844

中图分类号：

R75 [皮肤病学与性病学];

学科分类号：

100206 ;

摘要：

引用

页码：81 / 82

页数：2

共 20 条

[1] MULTIPLE TELANGIECTASIA RAYNAUDS PHENOMENON SCLERODACTYLY + SUBCUTANEOUS CALCINOSIS - SYNDROME MIMICKING HEREDITARY HEMORRHAGIC TELANGIECTASIA
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[5] Pulmonary capillary hemangiomatosis or hepatopulmonary syndrome in a patient with calcinosis, Raynaud's phenomenon, esophageal dysmotility, sclerodactyly and telangiectasia syndrome?
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[J]. CHINESE MEDICAL JOURNAL, 2020, 133 (02) : 243 - 244
[6] Pulmonary capillary hemangiomatosis or hepatopulmonary syndrome in a patient with calcinosis, Raynaud’s phenomenon, esophageal dysmotility, sclerodactyly and telangiectasia syndrome?
ShresthaBijayaLaxmi
JinYing-Kang
[J]. 中华医学杂志(英文版), 2020, 133 (02) : 243 - 244
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[J]. HNO, 2002, 50 (02) : 114 - +
[8] CONCURRENCE OF A VARIANT VONWILLEBRANDS DISEASE (VWD) AND HEREDITARY HEMORRHAGIC TELANGIECTASIA (HHT) IN A FAMILY
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[9] Primary localized cutaneous nodular amyloidosis associated with CREST (calcinosis, Raynaud's phenomenon, esophageal motility disorders, sclerodactyly, and telangiectasia) syndrome
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[10] A case of hereditary hemorrhagic telangiectasia (Rendu-Osler-Weber's disease) with dystrophic calcinosis cutis and retinal lesions
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[J]. JOURNAL OF DERMATOLOGY, 2002, 29 (08): : 512 - 515

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