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Hypermanganesemia with Dystonia Type 2: A Potentially Treatable Neurodegenerative Disorder: A Case Series in a Tertiary University Hospital
Importance: Hypermanganesemia with dystonia type 2 is a rare autosomal recessive neurodegenerative disorder characterized by the loss of previously acquired milestones, dystonia, parkinsonian features, a high serum manganese level, and characteristic neuroimaging findings such as bilateral and symme...
Autores principales: | Alhasan, Khalid A., Alshuaibi, Walaa, Hamad, Muddathir H., Salim, Suha, Jamjoom, Dima Z., Alhashim, Aqeela H., AlGhamdi, Malak Ali, Kentab, Amal Y., Bashiri, Fahad A. |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9497897/ https://www.ncbi.nlm.nih.gov/pubmed/36138644 http://dx.doi.org/10.3390/children9091335 |
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