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Updated: Oct 27, 2025

Targeted Next-generation Sequencing and Bioinformatics Pipeline to Evaluate Genetic Determinants of Constitutional Disease
Published on: April 4, 2018
C19orf12 mutation causing mitochondrial membrane-protein Associated Neurodegeneration masquerading as spastic
Rithvik Ramesh1, Anu Deenadayalu2, Shakya Bhattacharjee3
1Department of Neurology, Sri Ramachandra Medical College, Chennai, India.
Abstract:
Mitochondrial Membrane-protein Associated Neurodegeneration (MPAN) is a rare disease, caused by C19orf12 mutations and up to 29 different mutations have been described. We report a young woman presented with spastic paraparesis due to C19orf12 gene. MPAN presenting like Hereditary spastic paraplegia-43 is rare and the genetic mutation had been described only once in the literature.
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