Congenital Myaesthenic Syndromes Panel

Overview

Test Name
Congenital Myaesthenic Syndromes Panel
Test Code
NUE1011
Test Category
Gene Panels
Test Subcategory
Neurology
Disease(s) Targeted
Congenital Myaesthenic Syndromes
Who Is The Test For?
Patients with a family history, clinical suspicion, or diagnosis of congenital myaesthenia.
Test Approach

Whole exome sequencing (WES) with in silico gene panel analysis.

No. of Genes
27
Panel Content
Deliverables
Turnaround Time

~3-6 weeks*

Specimen Requirements

For detailed information about the sample requirements, please consult our clinical sample requirements page.

*Turnaround times are estimated from receipt of satisfactory specimen and test request form at the laboratory to release of clinical report. The turnaround time may vary depending on the nature of the specimen and the complexity of the investigation required. The above table is only a guideline and the complexity of a case and the requirement for further investigations may change this.

About Congenital Myaesthenic Syndromes

Congenital Myasthenic Syndromes are inherited disorders causing muscle weakness due to problems with nerve-to-muscle communication from birth.

Gene Panel Workflow

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