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Liddle Syndrome / Familial
Hypertension
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| Gene: |
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SCNN1B;
SCNN1G
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| Test: |
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Sequencing
of exon 13 of both SCNN1B and SCNN1G
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CPT Codes:
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83891 x 1
83898 x 4
83904 x 8
83909 x 8
83912 x 1 |
| Sensitivity: |
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Liddle Syndrome is a rare condition, and
series of patients screened for SCNN1B
or SCNN1G mutations have not been published. Our test panel is
designed to detect >99% of mutations published to date.
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| Cost: |
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$662 per individual
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| Turn
Around Time: |
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3
to 4 weeks |
| Special
Considerations: |
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Phenotypic
information is extremely helpful.
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| |
Click
here for Sample Requirements
Click Here for
Requisition and Billing forms
Click here for clinical information on Liddle Syndrome.
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