Primary hypoparathyroidism and multiple neuraxial involvement in mitochondrial disorder due to the variant m.15043G>A in MT-CYB

Affiliations

¹ Department of General Medicine, Burdwan Medical College & Hospital, Burdwan, West Bengal, India.
² Department of Neuromedicine, Bangur Institute of Neurosciences, Institute of Postgraduate Medical Education and Research & SSKM Hospital, Kolkata, West Bengal, India.
³ Department of General Medicine, Rajendra Institute of Medical Sciences, Ranchi, Jharkhand, India.
⁴ Department of Neurology, Krankenanstalt Rudolfstiftung, Messerli Institute, Vienna, Austria. Electronic address: fifigs1@yahoo.de.
⁵ Department of Medicine, Kamineni Institute of Medical Sciences, Narketpally, Nalgonda, Telangana, India.

Ritwik Ghosh et al. J Neurol Sci. 2020.

. 2020 Jul 15:414:116853.

doi: 10.1016/j.jns.2020.116853. Epub 2020 Apr 18.

¹ Department of General Medicine, Burdwan Medical College & Hospital, Burdwan, West Bengal, India.
² Department of Neuromedicine, Bangur Institute of Neurosciences, Institute of Postgraduate Medical Education and Research & SSKM Hospital, Kolkata, West Bengal, India.
³ Department of General Medicine, Rajendra Institute of Medical Sciences, Ranchi, Jharkhand, India.
⁴ Department of Neurology, Krankenanstalt Rudolfstiftung, Messerli Institute, Vienna, Austria. Electronic address: fifigs1@yahoo.de.
⁵ Department of Medicine, Kamineni Institute of Medical Sciences, Narketpally, Nalgonda, Telangana, India.

No abstract available

Keywords: Hereditary; Hypoparathyroidism; Lactic acidosis; Mitochondrial; Movement disorder; Multisystem disease; mtDNA.

Comment in

The m.15043G > A MT-CYB variant is not a pathogenic mtDNA variant.
Alston CL, Blakely EL, McFarland R, Taylor RW. Alston CL, et al. J Neurol Sci. 2020 Oct 15;417:116950. doi: 10.1016/j.jns.2020.116950. Epub 2020 May 29. J Neurol Sci. 2020. PMID: 32522371 Free PMC article. No abstract available.