Mirror Movements 2; Mrmv2

Table of contents:

Description
Related genes
Clinical Features
Incidence and onset information
Alternative Names
Researches and researchers
Gene Panels
Sources and references

Description

Mirror movements are involuntary movements of a side of the body that mirror intentional movements on the opposite side. Mild mirror movements are physiologic in young children and gradually disappear within the first decade of life, likely due to maturation of the motor network. Mirror movements that persist beyond age 10 years represent a rare disorder usually showing autosomal dominant inheritance with incomplete penetrance (summary by Depienne et al., 2012).For a discussion of genetic heterogeneity of mirror movements, see MRMV1 (OMIM ).

Genes related to Mirror Movements 2; Mrmv2

RAD51

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Clinical Features

Phenotypes and symptoms related to Mirror Movements 2; Mrmv2

Pain
Involuntary movements
Bimanual synkinesia

Incidence and onset information

— Currently we don't have prevalence information about this disease (Not enough data available about incidence and published cases.)
— No data available about the known clinical features onset.

Researches and researchers

Currently, we don't have any information about doctors, researches or researchers related to this disease. Please contact us if you would like to appear here.

Mirror Movements 2; Mrmv2 Recommended genes panels

Panel Name, Specifity and genes Tested/covered
Hereditary Myeloid Malignancy and Inherited Bone Marrow Failure Panel. By Genetic Services Laboratory University of Chicago (United States). RPL11, RPL15, RPL26, RPL35A, RPL5, RPS10, RPS19, RPS24, RPS26, RPS7, RUNX1, BLM, BRCA1, BRCA2, SRP72, TERC, TERT, TINF2, TP53, WAS , (...) View the complete list with 58 more genes Panel complete gene list RPL11, RPL15, RPL26, RPL35A, RPL5, RPS10, RPS19, RPS24, RPS26, RPS7, RUNX1, BLM, BRCA1, BRCA2, SRP72, TERC, TERT, TINF2, TP53, WAS, IKZF1, SAMD9, SAMD9L, NHP2, NOP10, VPS45, CBL, RTEL1, HAX1, POT1, CEBPA, SBDS, BRIP1, FANCL, SBF2, SLX4, CSF3R, G6PC3, UBE2T, ACD, NAF1, WRAP53, FANCI, CXCR4, USB1, PALB2, CTC1, DNAJC21, DKC1, ANKRD26, ELANE, ERCC4, ETV6, FANCA, FANCB, FANCC, FANCD2, FANCE, FANCF, FANCG, ALAS2, GATA1, GATA2, GFI1, MLH1, MPL, MSH2, MSH6, NBN, NF1, ATM, PARN, PAX5, PMS2, PTPN11, RAD51, RAD51C, RBM8A Specificity 2 % Genes 100 %
Breast cancer (sequence analysis of RAD51 gene). By CGC Genetics (Portugal). RAD51 Specificity 100 % Genes 100 %
Hereditary Ovarian Cancer. By Laboratory of Genetics BioTe21 Adam Master (Poland). BRCA1, BRCA2, TP53, BRIP1, MRE11, NBN, BARD1, RAD50, RAD51, RAD51C, RAD51D Specificity 10 % Genes 100 %
Fanconi Anemia Sequencing Panel with CNV Detection. By PreventionGenetics PreventionGenetics (United States). BRCA1, BRCA2, XRCC2, BRIP1, FANCL, FANCM, SLX4, UBE2T, FANCI, PALB2, ERCC4, FANCA, FANCB, FANCC, FANCD2, FANCE, FANCF, FANCG, MAD2L2, RAD51 , (...) View the complete list with 1 more genes Panel complete gene list BRCA1, BRCA2, XRCC2, BRIP1, FANCL, FANCM, SLX4, UBE2T, FANCI, PALB2, ERCC4, FANCA, FANCB, FANCC, FANCD2, FANCE, FANCF, FANCG, MAD2L2, RAD51, RAD51C Specificity 5 % Genes 100 %
Fanconi Anemia via RAD51/FANCR Gene Sequencing with CNV Detection. By PreventionGenetics PreventionGenetics (United States). RAD51 Specificity 100 % Genes 100 %
Mirror movements, familial congenital. By Centogene AG - the Rare Disease Company (Germany). RAD51 Specificity 100 % Genes 100 %
Breast ovarian cancer panel. By Centogene AG - the Rare Disease Company (Germany). STK11, TP53, CDH1, BRIP1, PALB2, MRE11, MSH6, NBN, ATM, BARD1, PTEN, RAD51, RAD51C Specificity 8 % Genes 100 %
Single gene testing RAD51. By CeGaT GmbH (Germany). RAD51 Specificity 100 % Genes 100 %

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Sources and references

You can check the following sources for additional information.

OMIM Rare Disease Symptoms Checker

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