Hypermagnesemia with Dystonia Type 2: Case Report of a New SLC30A10 Variant

Manganese-induced neurological disorder (HMNDYT1) is a rare condition characterized by the accumulation of manganese in the brain, leading to neurological symptoms such as difficulties in walking. This disorder arises due to genetic mutations affecting manganese transport and metabolism. Presented i...

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Bibliographic Details
Published in:	Journal of Pharmacy and Bioallied Sciences
Main Authors:	Fahad Alamr, Hadeel M. Alzahrani, Meelaf A. Alhomrani, Abdulrhman S. Alzhrani, Ayan Adel Abdullah Alghamdi, Atheer Awadh Alharthi
Format:	Article
Language:	English
Published:	Wolters Kluwer Medknow Publications 2024-12-01
Subjects:	basal ganglia pathology genetic disorders pediatric neurology polycythemia management whole exome sequencing
Online Access:	https://journals.lww.com/10.4103/jpbs.jpbs_809_24

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