Suppr超能文献

先天性角化不良:这种多系统疾病的两个病例。

Dyskeratosis congenita: two examples of this multisystem disorder.

作者信息

Womer R, Clark J E, Wood P, Sabio H, Kelly T E

出版信息

Pediatrics. 1983 Apr;71(4):603-9.

PMID:6601257
Abstract

Two brothers with the X-linked disorder, dyskeratosis congenita, are described. They showed the dermatologic triad of reticular hyperpigmentation, dystrophic nails, and leukoplakia oris as well as the other major feature of this disorder, aplastic anemia. Less common features observed included prenatal and postnatal growth retardation, mental retardation, elevated immunoglobulin levels, and gastrointestinal hemorrhage from mucosal ulceration. Previously unreported findings were intracranial calcifications and nutmeg-like cirrhotic changes of the liver. These brothers demonstrated that skeletal changes and bony fragility may predate anemia or steroid therapy. Although a DNA repair defect is postulated as a possible primary defect, cytogenetic studies revealed no evidence of increased chromosomal breakage.

摘要

本文描述了两名患有X连锁疾病先天性角化不良的兄弟。他们表现出网状色素沉着、甲营养不良和口腔黏膜白斑的皮肤三联征,以及该疾病的另一主要特征再生障碍性贫血。观察到的较少见特征包括产前和产后生长发育迟缓、智力障碍、免疫球蛋白水平升高以及黏膜溃疡引起的胃肠道出血。此前未报告的发现是颅内钙化和肝脏呈肉豆蔻样的肝硬化改变。这些兄弟表明骨骼变化和骨质脆弱可能早于贫血或类固醇治疗出现。尽管推测DNA修复缺陷可能是原发性缺陷,但细胞遗传学研究未发现染色体断裂增加的证据。

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