儿童原发性肾上腺功能不全的病因与诊断。

IF 1.5 4区 医学 Q4 ENDOCRINOLOGY & METABOLISM Journal of Clinical Research in Pediatric Endocrinology Pub Date : 2025-01-10 Epub Date: 2024-12-23 DOI:10.4274/jcrpe.galenos.2024.2024-6-24-S
Müge Atar, Leyla Akın
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引用次数: 0

摘要

原发性肾上腺功能不全(PAI)是一种需要及时诊断和开始治疗的危重疾病。由于各种潜在原因,包括肾上腺发育缺陷、对促肾上腺皮质激素(ACTH)的抵抗、自身免疫性原因和代谢问题,诊断可能具有挑战性。具体的诊断对于制定治疗计划和确定其他可能伴随的病理是必不可少的。生化研究、遗传分析和成像技术有助于建立具体的诊断。本循证指南包括导致PAI的具体诊断及其临床和遗传特征。它还提供了诊断时可遵循的循证步骤。
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The Causes and Diagnosis of Non-congenital Adrenal Hyperplasia Primary Adrenal Insufficiency in Children

Primary adrenal insufficiency (PAI) is a critical condition that requires prompt diagnosis and initiation of treatment. Diagnosis can be challenging due to various underlying causes, including defects in adrenal gland development, resistance to adrenocorticotropic hormone, autoimmune causes, and metabolic problems. A specific diagnosis is essential for developing a treatment plan and identifying other possible accompanying pathologies. Biochemical studies, genetic analyses, and imaging techniques are helpful in establishing a specific diagnosis. This evidence-based guideline includes the specific diagnoses that cause PAI and their clinical and genetic features. It also provides evidence-based steps to follow when making a diagnosis.

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来源期刊
Journal of Clinical Research in Pediatric Endocrinology
Journal of Clinical Research in Pediatric Endocrinology ENDOCRINOLOGY & METABOLISM-PEDIATRICS
CiteScore
3.60
自引率
5.30%
发文量
73
审稿时长
20 weeks
期刊介绍: The Journal of Clinical Research in Pediatric Endocrinology (JCRPE) publishes original research articles, reviews, short communications, letters, case reports and other special features related to the field of pediatric endocrinology. JCRPE is published in English by the Turkish Pediatric Endocrinology and Diabetes Society quarterly (March, June, September, December). The target audience is physicians, researchers and other healthcare professionals in all areas of pediatric endocrinology.
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