医学
内质网
血小板
超微结构
核糖体
包涵体
包裹体(矿物)
病理
免疫学
细胞生物学
遗传学
生物
人类学
核糖核酸
基因
社会学
大肠杆菌
作者
Eriko Yamazaki,Hiroshi Harano,Satoshi Fujisawa,Sou Kobayashi,K Ogawa,Yoshiaki Ishigatsubo
出处
期刊:PubMed
日期:2001-11-01
卷期号:42 (11): 1139-41
摘要
We report a Japanese family with Sebastian platelet syndrome. Twenty-one thrombocytopenic patients exhibited giant platelets and inclusion bodies in their granulocytes. They were thought to be related because they bore the same surname and lived within a localized area. None of them had additional clinical findings peculiar to Fechtner syndrome. Ultrastructural studies of the granulocytes were performed on four patients. The inclusion bodies in the granulocytes were different from those found in May-Hegglin anomaly, and consisted of ribosome clusters and rough endoplasmic reticula.
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