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病例报告:蒂特斯维尔血红蛋白:一例发绀的特殊病例。

Case Report: Hemoglobin titusville: a specific case of cyanosis.

作者信息

Zhang Meng, Wang Kai, Xu Xinyi, Ji Wei, Guo Ying, Gao Wei, Liu Tingliang

机构信息

Department of Cardiology, Shanghai Children's Medical Center, School of Medicine, Shanghai Jiao Tong University, Shanghai, China.

出版信息

Front Cardiovasc Med. 2025 Jun 17;12:1537704. doi: 10.3389/fcvm.2025.1537704. eCollection 2025.

Abstract

Hemoglobin Titusville is a rare low-oxygen-affinity hemoglobinopathy characterized by normal arterial partial pressure of oxygen but low oxygen saturation. In this study, we describe a case of hemoglobinopathy presenting as cyanosis. A 12-year-old female patient was admitted to the hospital with cyanosis and 87% blood oxygen saturation. Overall, the patient was healthy and preserved exercise tolerance. Upon admission, her arterial partial pressure of oxygen was 121 mmHg, and her blood oxygen saturation was 89.7%. First, the common causes were excluded, after which cardiovascular catheterization was performed. This detected no shunt between the systemic and pulmonary circulation. Finally, whole-exon sequencing confirmed a heterozygous mutation of the gene (g.227115G>A). In this study, we review the entire course of this case, providing scientific insight into this disease and a differential diagnosis of cyanosis.

摘要

蒂特斯维尔血红蛋白病是一种罕见的低氧亲和力血红蛋白病,其特征是动脉血氧分压正常但血氧饱和度低。在本研究中,我们描述了一例以发绀为表现的血红蛋白病病例。一名12岁女性患者因发绀和87%的血氧饱和度入院。总体而言,该患者身体健康,运动耐量良好。入院时,她的动脉血氧分压为121 mmHg,血氧饱和度为89.7%。首先排除了常见病因,之后进行了心血管导管检查。检查未发现体循环和肺循环之间存在分流。最后,全外显子测序证实该基因存在杂合突变(g.227115G>A)。在本研究中,我们回顾了该病例的全过程,为这种疾病及发绀的鉴别诊断提供了科学见解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4d86/12209305/798979c7f3be/fcvm-12-1537704-g001.jpg

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