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...

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Detalles Bibliográficos
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.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Article
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

Internet

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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