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姐妹俩患婴儿特发性动脉钙化且临床表现异常

Idiopathic arterial calcification of infancy with unusual clinical presentations in sisters.

作者信息

Stanley R J, Edwards W D, Rommel D A, Smithson W A

机构信息

Department of Pathology, Mayo Clinic, Rochester, Minnesota.

出版信息

Am J Cardiovasc Pathol. 1988;2(3):241-5.

PMID:3219207
Abstract

Two cases of idiopathic arterial calcification of infancy that occurred in sisters are reported. One patient died at age 14 months after a protracted course characterized by the nephrotic syndrome, blood chemistry abnormalities, hypertension, seizures, and a microangiopathic hemolytic anemia. Her sister died at age 3 weeks after a precipitous illness that initially was misinterpreted at autopsy as Reye's syndrome.

摘要

本文报告了两例发生在姐妹身上的婴儿特发性动脉钙化病例。其中一名患者在经历了以肾病综合征、血液化学异常、高血压、癫痫发作和微血管病性溶血性贫血为特征的漫长病程后,于14个月大时死亡。她的妹妹在3周大时因一场急病去世,尸检最初误诊为瑞氏综合征。

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