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April 1, 2026International Journal of Developmental Neuroscience

Long‐Term Outcomes in Tyrosine Hydroxylase Deficiency: A Case Series of Four Paediatric Patients

Rong Ren Aiyun Yuan Mei Hou Guangjin Luo Xiaoming Yu Z X Chen Yedan Liu

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Implication

Case series examines long-term outcomes of dopa-responsive dystonia in children, suggesting key clinical insights.

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Cite This Study

Ren et al. (2026) studied this question.

synapsesocial.com/papers/69e320fd40886becb65402e7 https://doi.org/10.1002/jdn.70125

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Keep reading

Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context:

1Consensus Guideline for the Diagnosis and Treatment of Tyrosine Hydroxylase ( <scp>TH</scp> ) Deficiency2025
2Dopa‐responsive dystoniaCohort Study · 1991 · 244 citations
3Genetic analysis reveals phenotypic variability in three Colombian families with dopa-responsive dystonia: novel genotype-phenotype correlationsOriginal Research · 2026
4Three Cases of Levodopa–Carbidopa Responsive Nocturnal Akinesis in Male Children of an Inbred Family in Rural Baluchistan, PakistanOriginal Research · 2026
5Tyrosine Hydroxylase Deficiency Impairs <scp>TH</scp> Axonal Transport, Brain Function, and Neuronal PlasticityOriginal Research · 2026