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| Test Name: | VHL Gene Comprehensive Study |
| Compliance: | LDT, RUO |
| Test Description: | VHL is the gene known to be associated with VHL syndrome.VHL syndrome is is inherited in an autosomal dominant manner and characterized by hemangioblastomas of the brain, spinal cord, and retina; renal cysts and clear cell renal cell carcinoma; pheochromocytoma; and endolymphatic sac tumors. |
| Methodology: | PCR-Sanger sequencing analysis and Deletion/Duplication analysis of VHL gene |
| Gene Name: | VHL |
| Protein Name: | |
| Specimen Requirements: | EDTA Blood (5mL) |
| Storage Condition: | Ambient Temperature |
| Turn Around Time: | 20 working days from day of specimen received |
| OMIM: | |
| Genetic Home Reference: | |
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This notice describes how medical information about you may be used and disclosed.
Personal health information or related information released to HKMPDC relating to the services requested may be subjected to re-disclosure by HKMPDC to health care providers, such as doctors, nurses, and others involved in the delivery of the services.
We may also disclose medical information about you to authorised public health or government officials for public health activities as required by law and accreditation body.
Copyright © 2013 香港分子病理檢驗中心 Hong Kong Molecular Pathology Diagnostic Centre Limited (HKMPDC). All Rights Reserved.
Information Updated 1 July, 2023.
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