Cerebral Infarction in Three Infant Cases of Congenital Adrenal Hyperplasia

Katsuhiko Tachibana; Hatae Maesaka; Seizo Suwa; Masanori Adachi; Toshihisa Okada

首页> 外文期刊>Clinical Pediatric Endocrinology >Cerebral Infarction in Three Infant Cases of Congenital Adrenal Hyperplasia

【24h】

Cerebral Infarction in Three Infant Cases of Congenital Adrenal Hyperplasia

机译：三例婴儿先天性肾上腺皮质增生病例的脑梗死

获取原文

掌桥外文数据库（机构版） >>

开具论文收录证明 >>

文献代查 >>

页面导航

摘要
著录项
相似文献
相关主题

摘要

The objective of this study was to discuss the etiology of cerebral infarction in three cases of congenital adrenal hyperplasia (CAH) based on detailed individual case reports. Patients consisted of three children, two female, one male, 3y, 2y 6mon., and 3y 6mon, with CAH who developed cerebral infarction. The possibility of cerebral infarction following hypoglycemia due to adrenal insufficiency can be considered but the evidence is not conclusive. The combination of cerebral infarction, a rare condition among children, and CAH might not be accidental but suggests the possibility that CAH itself or treatment with glucocorticoid and/or mineralocorticoid or an inadequate treatment under stressful condition may be the cause of the cerebral infarction.

机译：这项研究的目的是在详细的个别病例报告的基础上，讨论3例先天性肾上腺皮质增生（CAH）病例的脑梗死病因。患者由3名儿童组成，其中2名女性，1名男性，3y，2y 6mon和3y 6mon患有发展为脑梗死的CAH。可以考虑由于肾上腺功能不全引起的低血糖后脑梗死的可能性，但证据尚无定论。脑梗死，儿童罕见病和CAH的结合可能不是偶然的，但表明CAH本身或糖皮质激素和/或盐皮质激素的治疗或在压力条件下的治疗不足可能是脑梗死的原因。

著录项

来源
《Clinical Pediatric Endocrinology》 |1997年第1期|共4页
作者
Katsuhiko Tachibana; Hatae Maesaka; Seizo Suwa; Masanori Adachi; Toshihisa Okada;
展开▼
作者单位

展开▼
收录信息
原文格式 PDF
正文语种
中图分类医学免疫学;
关键词

相似文献

外文文献
中文文献
专利

1. Absence of Testicular Adrenal Rest Tumors in Newborns, Infants, and Toddlers with Classical Congenital Adrenal Hyperplasia (vol 92, pg 157, 2019) [J] . Hormone research in p?diatrics . 2019,第3期

机译：在新生儿，婴儿和幼儿中没有睾丸肾上腺静肿瘤，具有古典先天性肾上腺增生（Vol 92，PG 157,2019）
2. Absence of Testicular Adrenal Rest Tumors in Newborns, Infants, and Toddlers with Classical Congenital Adrenal Hyperplasia [J] . Hormone research in p?diatrics . 2019,第3期

机译：在新生儿，婴儿和幼儿中缺乏睾丸肾上腺静止肿瘤，具有古典先天性肾上腺增生
3. Lipoid congenital adrenal hyperplasia by steroidogenic acute regulatory protein (STAR) gene mutation in an Italian infant: an uncommon cause of adrenal insufficiency [J] . Carla Bizzarri, Elisa Pisaneschi, Mafalda Mucciolo, Italian journal of pediatrics . 2017,第1期

机译：在意大利婴儿中，类固醇生成性急性调节蛋白（STAR）基因突变引起的类脂性先天性肾上腺增生：肾上腺功能不全的常见原因
4. Effects of Adrenal Steroids on the Bone Metabolism of Children with Congenital Adrenal Hyperplasia [C] . KAREN LIN-SU, MARIA I. NEW Conference on Skeletal Biology and Medicine . 2007

机译：肾上腺类固醇对先天性增生患儿骨代谢的影响
5. Parental management of adrenal crisis in children with congenital adrenal hyperplasia. [D] . Fleming, Louise Kathleen. 2016

机译：先天性肾上腺皮质增生患儿的肾上腺危机的父母管理。
6. Plasma 17-hydroxyprogesterone in newborn infants with congenital adrenal hyperplasia and in infants with normal adrenal function [O] . Shelia M. Atherden, A. T. Edmunds, D. B. Grant 1974

机译：先天性肾上腺皮质增生的新生儿和肾上腺功能正常的婴儿的血浆17-羟孕酮
7. Plasma 17-hydroxyprogesterone in newborn infants with congenital adrenal hyperplasia and in infants with normal adrenal function [O] . Atherden, Shelia M., Edmunds, A. T., Grant, D. B. 1974

机译：先天性肾上腺皮质增生的新生儿和肾上腺功能正常的婴儿的血浆17-羟孕酮

Cerebral Infarction in Three Infant Cases of Congenital Adrenal Hyperplasia

摘要

著录项

相似文献

相关主题

期刊订阅