Tyrosine hydroxylase deficiency in a child initially misdiagnosed as cerebral palsy combined with epilepsy
Author:
Publisher
Springer Science and Business Media LLC
Link
https://link.springer.com/content/pdf/10.1007/s13760-024-02631-9.pdf
Reference4 articles.
1. Dong HY, Feng JY, Yue XJ et al (2020) Dopa-responsive dystonia caused by tyrosine hydroxylase deficiency: three cases report and literature review. Med (Baltim) 99(33):e21753. https://doi.org/10.1097/MD.0000000000021753
2. Nygaard G, Szigetvari PD, Grindheim AK et al (2021) Personalized Medicine to Improve Treatment of Dopa-Responsive Dystonia-A Focus on Tyrosine Hydroxylase Deficiency. J Pers Med 11(11):1186. https://doi.org/10.3390/jpm11111186
3. Himmelmann K, Horber V, Sellier E et al (2021) Surveillance of cerebral palsy in Europe (SCPE) collaboration. Neuroimaging patterns and function in cerebral palsy-application of an MRI classification. Front Neurol 11:617740. https://doi.org/10.3389/fneur.2020.617740
4. Santana Almansa A, Gable DL, Frazier Z et al (2024) Clinical utility of a genetic diagnosis in individuals with cerebral palsy and related motor disorders. Ann Clin Transl Neurol 11(2):251–262. https://doi.org/10.1002/acn3.51942
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