Suppr超能文献

一名青少年透明纤维瘤病患者的皮肤胶原蛋白缺陷。

Skin collagen defects in a patient with juvenile hyaline fibromatosis.

作者信息

Lubec B, Steinert I, Breier F, Jurecka W, Pillwein K, Fang-Kircher S

机构信息

Department of Paediatrics (Neonatology), University of Vienna, Austria.

出版信息

Arch Dis Child. 1995 Sep;73(3):246-8. doi: 10.1136/adc.73.3.246.

Abstract

Juvenile hyaline fibromatosis is a rare disorder characterised by multiple subcutaneous tumours, gum hypertrophy, muscle weakness, and flexion contractures of the large joints. Histology shows an abundance of a homogenous, amorphous, acidophilic extracellular matrix in which spindle shaped cells are embedded forming minute streaks. It has been previously suggested that collagen abnormalities may be involved. A 14 month old girl with this syndrome is described in whom postmortem western blot studies were performed. These studies revealed an absent pro-alpha 2(I) chain and an absent collagen type III chain in skin but not in the other organs examined.

摘要

青少年透明纤维瘤病是一种罕见的疾病,其特征为多发性皮下肿瘤、牙龈肥大、肌肉无力以及大关节的屈曲挛缩。组织学显示有大量均匀、无定形、嗜酸性的细胞外基质,其中嵌入梭形细胞形成微小条纹。此前有人提出可能涉及胶原蛋白异常。本文描述了一名患有该综合征的14个月大女孩,对其进行了死后蛋白质印迹研究。这些研究显示,皮肤中缺乏前α2(I)链和III型胶原链,但在所检查的其他器官中未发现。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aba4/1511266/3e37a8d52dbd/archdisch00621-0068-a.jpg

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