Extreme Early-onset Hypertension Panel

Nephrology

Extreme Early-onset Hypertension Panel

Overview

Test Name
Extreme Early-onset Hypertension Panel
Test Code
NEE1007
Test Category
Gene Panels
Test Subcategory
Nephrology
Disease(s) Targeted
Extreme Early onset hypertension
Who Is The Test For?
Patients with a family history, clinical suspicion, or diagnosis of extreme early onset hypertension.
Test Approach

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

No. of Genes
15
Panel Content
CUL3, CYP11B1, CYP11B2, CYP17A1, HSD11B2, KCNJ5, KLHL3, MTX2, NR3C1, NR3C2, SCNN1B, SCNN1G, TTC21B, WNK1, WNK4
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 Extreme Early onset hypertension

Extreme Early Onset Hypertension (EEOHT) is severe high blood pressure developing in adulthood, often before age 30, with a strong genetic basis, unlike common essential hypertension which involves complex polygenic factors and lifestyle. Prevalence varies, but these rare, single-gene conditions often involve variants in genes regulating aldosterone and salt balance, such as in Familial Hyperaldosteronism (inherited in an autosomal dominant manner and associated with KCNJ5 gene variants) or Pseudohypoaldosteronism type II (frequently inherited in an autosomal dominant manner and linked to CUL3, KLHL3, WNK1, and WNK4 genes).

Gene Panel Workflow

Order a test using our clinical portal

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