Suppr超能文献

[常染色体隐性白化丘疹型营养不良性大疱性表皮松解症]

[Autosomal recessive albopapuloid dystrophic epidermolysis bullosa].

作者信息

Ramelet A A, Boillat C

出版信息

Dermatologica. 1985;171(6):397-406.

PMID:4092794
Abstract

Albopapules are usually considered as pathognomonic lesions of Pasini's epidermolysis bullosa, which is dominantly transmitted. Herein, we are reporting 3 cases of recessively inherited epidermolysis bullosa with albopapules. The clinical, histological and ultrastructural features are described. It is concluded that the presence of albopapules is not necessarily a safe criterion for the diagnosis of Pasini's epidermolysis bullosa.

摘要

白色丘疹通常被认为是帕西尼大疱性表皮松解症的特征性损害,该疾病为常染色体显性遗传。在此,我们报告3例伴有白色丘疹的隐性遗传性大疱性表皮松解症病例。描述了其临床、组织学和超微结构特征。得出的结论是,白色丘疹的存在不一定是诊断帕西尼大疱性表皮松解症的可靠标准。

相似文献

2
[Albopapuloid epidermolysis bullosa (Pasini's disease)].
Med Cutan Ibero Lat Am. 1981;9(4):307-10.
9
Lethal epidermolytic epidermolysis bullosa: a new autosomal recessive type of epidermolysis bullosa.
Br J Dermatol. 1985 Aug;113(2):135-43. doi: 10.1111/j.1365-2133.1985.tb02055.x.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验