eISSN: 2084-9869
ISSN: 1233-9687
Polish Journal of Pathology
Current issue Archive Manuscripts accepted About the journal Supplements Editorial board Abstracting and indexing Subscription Contact Instructions for authors Ethical standards and procedures
Editorial System
Submit your Manuscript
SCImago Journal & Country Rank
3/2020
vol. 71
 
Share:
Share:
abstract:
Letter to the Editor

Diagnosing MERRF requires clinical and genetic evidence

Josef Finsterer
1

1.
Neurological Department, Klinik Landstrasse, Messerli Institute, Vienna, Austria
Pol J Pathol 2020; 71 (3): 283-284
Online publish date: 2020/10/25
View full text Get citation
 
PlumX metrics:
The interesting case about a patients with myoclonic epilepsy with ragged-red fibers (MERRF) syndrome due to the variant m.8344A>G with a heteroplasmy rate of 95% reported by Felczak et al. expands the phenotypic spectrum of MERRF syndrome. The authors reported a pituitary adenoma, calcium deposits in arterial walls, and an intra-cerebral lipoma in the corpus callosum in their patient. Shortcomings of the study are that the diagnostic criteria for MERRF were not accomplished, that the patient should be rather diagnosed as a mitochondrial, multiorgan disorder syndrome (MIMODS), that no pedigree and heteroplasmy rates in first degree relative were provided, that hormone levels were not provided despite obvious endocrinological involvement, and that no serum or cerebrospinal fluid (CSF) lactate levels were reported.
keywords:

mtDNA, mitochondrial, MERRF, m8344A>G, multisystem, MIMODS

Quick links
© 2024 Termedia Sp. z o.o.
Developed by Bentus.