Au-Kline综合征伴一种新变异的女孩在夏季表现为热不耐:一例报告和文献复习

Kazuki Suemune, Hiroshi Yamaguchi, Hiroaki Hanafusa, Ming Juan Ye, Kandai Nozu, Hiroaki Nagase
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摘要

au - kline综合征(AKS)的特点是中重度智力障碍、张力低下和明显的特征相。其他特征,如心脏畸形、进食困难、肾积水、高疼痛耐受性、反复发热、异常出汗和热不耐受,也有报道。然而,我们对AKS耐热性的了解仍然有限。目的我们报告一例罕见的AKS病例,该病例发生在一名3岁的女孩,她在夏季因热不耐受而出现口服摄入不良。此外,我们对AKS进行了详细的回顾,并调查了AKS患者报告的热不耐受程度。方法为了评价HNRNPK变异体患者的“耐热性”,通过检索PubMed数据库,查阅英文文献中报道的HNRNPK变异体患者的病例。结果共鉴定出456篇。我们全面回顾了描述HNRNPK变异病例的摘要和精选文章,包括两篇原创文章、八份临床病例报告和两封致编辑的信。该队列包括23名男性和23名女性HNRNPK变异患者。17例患者携带错义变体,27例携带截断变体,2例携带内含子变体。所有病例的所有变异都是从头开始的。在这篇综述中,我们没有发现热不耐受的病例报告。结论我们发现了一种新的与异常出汗引起的热不耐受症状相关的AKS HNRNPK变异。AKS的热不耐受是否极为罕见或被低估尚不清楚,需要进一步调查。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Au-Kline syndrome with a novel variant in a girl presenting with heat intolerance in the summer: A case report and literature review

Background

Au-Kline syndrome (AKS) is characterized by moderate-to-severe intellectual disability, hypotonia, and distinctive characteristic facies. Other features, such as cardiac malformations, feeding difficulties, hydronephrosis, high pain tolerance, recurrent fever, abnormal sweating, and heat intolerance, have also been reported. However, our understanding of the heat tolerance of AKS remains limited.

Objective

We present a rare case of AKS in a 3-year old girl who presented with poor oral intake during the summer due to heat intolerance. Furthermore, we conducted a detailed review of AKS and investigated the extent to which heat intolerance was reported in patients with AKS.

Methods

To evaluate the “heat intolerance” in patients with HNRNPK variants, the literature in English was reviewed for cases reported as patients with HNRNPK variants by searching the PubMed database.

Results

A total of 456 articles were identified. We thoroughly reviewed the abstracts and selected articles describing cases with variants in HNRNPK, including two original articles, eight clinical case reports, and two letters to the editor. The cohort consisted of 23 male and 23 female patients with HNRNPK variants. Seventeen patients harbored missense variants, 27 harbored a truncating variant, and two harbored an intron variant. All variants in all the cases were de novo. In this review, we found no reported cases of heat intolerance.

Conclusion

We identified a novel HNRNPK variant of AKS associated with heat intolerance symptoms caused by abnormal sweating. Whether heat intolerance in AKS is extremely rare or underreported remains unclear, and further investigation is required.
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