H 综合征：婴儿期发病的糖尿病是这种罕见的自身炎症综合征的表现形式

Q4 Medicine

Journal of Clinical and Translational Endocrinology: Case Reports Pub Date : 2024-04-06 DOI:10.1016/j.jecr.2024.100165

Nosrat Ghaemi , Sara Shirdelzadeh , Mahdieh Vahedi , Samaneh Noroozi Asl , Sepideh Bagheri

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引用次数: 0

摘要

H综合征是一种非常罕见的自身炎症综合征，其特征是以字母H开头的一系列症状：多毛、色素沉着、高脂血症、高血糖、性腺功能减退、肝肿大、听力减退、心脏异常和身高矮小。在这里，我们报告了一名被诊断患有H综合征的14岁男孩，他从2岁起就开始接受糖尿病治疗。

本文章由计算机程序翻译，如有差异，请以英文原文为准。

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H syndrome: Infantile onset diabetes as presentation of this rare auto-inflammatory syndrome

H syndrome is a very rare auto inflammatory syndrome which is characterized by a constellation of symptoms mostly beginning with the letter H. Hypertrichosis, Hyperpigmentation, Hyperlipidemia, Hyperglycemia, Hypogonadism, Hepatomegaly, Hearing loss, Heart anomalies and short Height.

Here we report a 14 years old boy with the diagnosis of H syndrome who was being treated for diabetes since he was 2 years old.

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来源期刊

Journal of Clinical and Translational Endocrinology: Case Reports Medicine-Endocrinology, Diabetes and Metabolism

CiteScore

1.10

自引率

0.00%

发文量

审稿时长

27 weeks

期刊介绍： The journal publishes case reports in a variety of disciplines in endocrinology, including diabetes, metabolic bone disease and osteoporosis, thyroid disease, pituitary and lipid disorders. Journal of Clinical & Translational Endocrinology Case Reports is an open access publication.