Transient Hyperphosphatasemia in a Child with Autism Spectrum Disorder.

Q3 Medicine
Štěpán Kutílek, Eva Rondziková-Mlynarčíková, Kamila Pečenková, Richard Pikner, Tomáš Šmída, Eva Sládková, Tomáš Honzík, Hana Kolářová, Martin Magner
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Abstract

Introduction: Autism spectrum disorder (ASD) is a neurodevelopmental disorder characterized by deficits in social communication and the presence of restricted interests and repetitive behaviors. Transient hyperphosphatasemia of infancy and early childhood (THI) is a benign laboratory disorder characterized by transiently extremely elevated activity of serum alkaline phosphatase (S-ALP).

Case report: We present a 21-month-old girl with a right leg limp, most probably due to reactive arthritis after febrile viral infection, and deterioration of psychomotor development with concomitant transient elevation of S-ALP (61.74 μkat/L; normal 2.36-7.68 μkat/L). Normal values of serum creatinine, aspartate-aminotransferase, alanin-aminotransferase, calcium, phosphate, together with normal wrist X-ray ruled out rickets or other bone or hepatic cause of high S-ALP. The S-ALP gradually decreased within 3 months, thus fulfilling the THI criteria. Screening for inborn errors of metabolism was negative and meticulous neurologic, psychologic and psychiatric assessment pointed to the diagnosis of autism spectrum disorder (ASD). There was no causal relationship between THI and ASD, as high S-ALP was an accidental and transient finding within the routine laboratory assessment. However, when THI occurs in a child with an onset of a new disorder, or with a pre-existing bone or liver disease, it might seriously concern the physician.

Conclusion: Children with THI should be spared from extensive evaluations and unnecessary blood draws.

自闭症谱系障碍儿童的短暂性高磷酸血症。
简介:自闭症谱系障碍(Autism spectrum disorder, ASD)是一种神经发育障碍,其特征是社会沟通缺陷、兴趣受限和重复性行为。婴幼儿短暂性高磷酸血症(THI)是一种以血清碱性磷酸酶(S-ALP)活性短暂性极度升高为特征的良性实验室疾病。病例报告:我们报告了一个21个月大的女婴,右腿跛行,最可能是由于发热性病毒感染后的反应性关节炎,精神运动发展恶化并伴有S-ALP短暂升高(61.74 μkat/L;正常2.36-7.68 μkat/L)。血清肌酐、天冬氨酸转氨酶、丙氨酸转氨酶、钙、磷酸盐值正常,加上腕部x线检查正常,排除佝偻病或其他骨或肝性高S-ALP原因。S-ALP在3个月内逐渐下降,符合THI标准。先天性代谢异常的筛查结果为阴性,细致的神经、心理和精神病学评估指向自闭症谱系障碍(ASD)的诊断。THI和ASD之间没有因果关系,因为高S-ALP是在常规实验室评估中偶然和短暂的发现。然而,当THI发生在患有新疾病的儿童身上,或者患有先前存在的骨骼或肝脏疾病时,可能会引起医生的严重关注。结论:THI患儿应避免广泛的评估和不必要的抽血。
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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来源期刊
Acta medica (Hradec Kralove)
Acta medica (Hradec Kralove) Medicine-Medicine (all)
CiteScore
1.10
自引率
0.00%
发文量
8
审稿时长
20 weeks
期刊介绍: Acta Medica (Hradec Králové) is a multidisciplinary medical journal published by the Faculty of Medicine in Hradec Králové - Karolinum Press, the publishing house of Charles University. The journal is peer-reviewed and published quarterly in both paper and electronic form. The language of Acta Medica is English. Offerings include review articles, original articles, brief communications, case reports, announcements and notices. The journal was founded in 1958 under the title "A Collection of Scientific Works of the Charles University Faculty of Medicine in Hradec Kralove."
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