Clinical Reasoning: A 10-Year-Old Boy With Progressive Tremor, Insomnia, and Autonomic Dysfunction

A 10-year-old boy developed progressive tremor, insomnia, and autonomic dysfunction after an upper respiratory tract infection. Initial workup, including brain MRI, CSF analysis, and antibody screening, was unremarkable. By the third month of illness, brain MRI revealed multiple hyperintensities on fluid-attenuated inversion recovery sequences. Empiric immunotherapy led to partial clinical and radiologic improvement. However, neurologic deterioration continued despite subsequent immunosuppressive treatment, and follow-up imaging demonstrated progressive cerebral atrophy. <sup>18</sup>F-fluorodeoxyglucose PET revealed marked bilateral thalamic hypometabolism, providing a pivotal clue that redirected the diagnostic approach. Definitive diagnosis was ultimately established through targeted genetic analysis. This case underscores the importance of maintaining a broad differential diagnosis in pediatric patients presenting with progressive neurologic decline, even in the context of transient inflammatory or immune-appearing features. It also highlights the diagnostic value of genetic testing when conventional investigations are inconclusive.

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Publication Details

Journal
Neurology
Published
2025-10-17
DOI
https://doi.org/10.1212/wnl.0000000000214297
Primary Topic
Glycogen Storage Diseases and Myoclonus
Type
article
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0.00
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article

Clinical Reasoning: A 10-Year-Old Boy With Progressive Tremor, Insomnia, and Autonomic Dysfunction

Yihao Wang, Liyong Wu, Zhongyun Chen, Rui Liu
Neurology
Glycogen Storage Diseases and Myoclonus
article

Clinical Reasoning: A 10-Year-Old Boy With Progressive Tremor, Insomnia, and Autonomic Dysfunction

Yihao Wang, Liyong Wu, Zhongyun Chen, Rui Liu
article en

Abstract

A 10-year-old boy developed progressive tremor, insomnia, and autonomic dysfunction after an upper respiratory tract infection. Initial workup, including brain MRI, CSF analysis, and antibody screening, was unremarkable. By the third month of illness, brain MRI revealed multiple hyperintensities on fluid-attenuated inversion recovery sequences. Empiric immunotherapy led to partial clinical and radiologic improvement. However, neurologic deterioration continued despite subsequent immunosuppressive treatment, and follow-up imaging demonstrated progressive cerebral atrophy. <sup>18</sup>F-fluorodeoxyglucose PET revealed marked bilateral thalamic hypometabolism, providing a pivotal clue that redirected the diagnostic approach. Definitive diagnosis was ultimately established through targeted genetic analysis. This case underscores the importance of maintaining a broad differential diagnosis in pediatric patients presenting with progressive neurologic decline, even in the context of transient inflammatory or immune-appearing features. It also highlights the diagnostic value of genetic testing when conventional investigations are inconclusive.

NeurologyVol. 105(9)
Capital Medical University (CN)
Openalex Percentile: Top 57%
Glycogen Storage Diseases and Myoclonus
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