Severe axonal Charcot-Marie-Tooth disease with proximal weakness caused by de novo mutation in the MORC2 gene

Result code in IS VaVaI

<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00064203%3A_____%2F16%3A10323444" target="_blank" >RIV/00064203:_____/16:10323444 - isvavai.cz</a>

Alternative codes found

RIV/00216208:11130/16:10323444

Result on the web

<a href="http://dx.doi.org/10.1093/brain/awv411" target="_blank" >http://dx.doi.org/10.1093/brain/awv411</a>

DOI - Digital Object Identifier

<a href="http://dx.doi.org/10.1093/brain/awv411" target="_blank" >10.1093/brain/awv411</a>

Result language

angličtina

Original language name

Severe axonal Charcot-Marie-Tooth disease with proximal weakness caused by de novo mutation in the MORC2 gene

Original language description

It was with great interest that we read the article on advanced access by Sevilla et al. (2015) regarding axonal Charcot-Marie-Tooth (CMT2) disease caused by mutations in the MORC2 gene. Through whole-exome sequencing in a Spanish four generation CMT2 family with autosomal dominant pattern of inheritance, the authors identified the mutation p.R190W in the MORC2 gene as the cause of the disease. It was the only variant detected by whole-exome sequencing that segregated with the disease in the family. Afterwards, they tested an additional 52 patients with axonal Charcot-Marie-Tooth and found mutations in the MORC2 gene in two additional families, one with different de novo mutation and the second with the same p.R190W mutation, also de novo. Here, we would like to report another patient with the p.R190W mutation in the MORC2 gene and thus confirm the causality of this gene for the severe CMT2 with striking proximal weakness. Also, we would like to show that the p.R190W mutation is a hot spot and probably the most frequent mutation in this gene. Immediately after we became aware of this newly discovered gene, we detected this mutation by re-examining older whole-exome sequencing data in one of our patients. This observation may have consequences for clinical DNA diagnostics because the phenotype, despite being probably rare, seems to be clinically recognizable and selected patients may first be tested for this mutation. This study was approved by the ethics committee of University Hospital Motol and informed consent was obtained from the patient according to the Declaration of Helsinki.

Czech name

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Czech description

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Type

J_x - Unclassified - Peer-reviewed scientific article (Jimp, Jsc and Jost)

CEP classification

FH - Neurology, neuro-surgery, nuero-sciences

OECD FORD branch

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Project

<a href="/en/project/NV15-33041A" target="_blank" >NV15-33041A: Massive parallel sequencing of genes related to infantile epilepsies and epileptic encephalopathies for diagnostics of epilepsy in Czech patients.</a><br>

Continuities

P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)<br>I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace

Publication year

2016

Confidentiality

S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Name of the periodical

Brain

ISSN

0006-8950

e-ISSN

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Volume of the periodical

139

Issue of the periodical within the volume

4

Country of publishing house

GB - UNITED KINGDOM

Number of pages

4

Pages from-to

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UT code for WoS article

000374234900006

EID of the result in the Scopus database

2-s2.0-84964502174