Hereditary Vitreoretinopathy Panel
Hereditary Vitreoretinopathy Panel
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€29.00 EUR
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€29.00 EUR
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This product is only meant for customers who already purchased a MyGenome Test
HV are a group of congenital retina and vitreous degeneration, caused by genetic mutations in more than 20 genes and is characterazed by high risk of retinal detachment, early cataract, optically empty vitreous and neovascularization. Among involved genes we can found those codying for collagen and for potassium channel.
This panel is designed for those with a family history of hereditary vitreoretinopathies or symptoms of including conditions such as early cataract and retinal detachment.
The analysis takes into consideration the mutation of germline DNA, it investigates SNP and Indel mutations up to 150 bp.
List of main conditions:
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HV are a group of congenital retina and vitreous degeneration, caused by genetic mutations in more than 20 genes and is characterazed by high risk of retinal detachment, early cataract, optically empty vitreous and neovascularization. Among involved genes we can found those codying for collagen and for potassium channel.
This panel is designed for those with a family history of hereditary vitreoretinopathies or symptoms of including conditions such as early cataract and retinal detachment.
The analysis takes into consideration the mutation of germline DNA, it investigates SNP and Indel mutations up to 150 bp.
- Available in less than 24 hours
- Based on Whole Genome Sequencing
- More than 20 genes analyzed
- Investigates SNP and Indel mutations up to 150 bp
List of main conditions:
- Familial Exudative Vitreoretinopathy
- Stickler Syndrome
- Snowflake Vitreoretinal Degeneration
This product is only meant for customers who already purchased a MyGenome Test