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Tests Currently Offered
Requisition
Form (pdf format)
Requisition
Form (Word format)
Price List (pdf format)
Price List (Word format)
New Test Development
CAP / CLIA Certificates
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PreventionGenetics offers
a steadily expanding menu of Clinical DNA tests. Our laboratory is CAP/CLIA
certified. Please use the Requisition
Form when ordering tests.
Click on the links in the following list for test descriptions and test
prices.
Substantial price discounts on our Clinical Tests are
available for large test volumes. Please contact us about quantity discounts.
Clinical DNA testing at PreventionGenetics is offered
to patients only through physicians, Ph.D. clinical geneticists or genetic
counselors. We do not provide clinical testing directly to patients.
DNA
banking is also available from PreventionGenetics. Long-term,
secure storage of a DNA sample from patients is an excellent first
step in clinical genetics. We provide isolation and quantitation
of DNA, secure storage at two separate locations, and withdrawal
services. At this time, we are offering free DNA Banking to any
patient that orders a full gene sequencing test.
PreventionGenetics believes that it is in the best interest
of all people to maximize knowledge of their genomes. Our company aims
to provide comprehensive DNA banking and genome-wide DNA testing for health
care. This approach will yield low costs and high quality results. Please
contact us to discuss the establishment of a DNA Bank and genome-wide
DNA testing for your patients.
Tests
Currently Offered By Disease
Click on the links in the following list for test descriptions, test
prices and CPT codes.
Autosomal Recessive Polycystic Kidney Disease (PKHD1) |
Bernard-Soulier Syndrome (GP1BA, GP1BB, GP9)) |
Cardio-Facio-Cutaneous
Syndrome (BRAF, KRAS, MAP2K1, MAP2K2) |
| Cavernous Malformations
(KRIT1/CCM1, CCM2, PDCD10/CCM3) |
| Central Core Disease (RYR1) |
| CHARGE Syndrome (CHD7) |
| Congenital Muscular Dystrophy (FCMD, FKRP, LAMA2, LARGE) |
| Costello Syndrome
(HRAS) |
| Cystic Fibrosis
(CFTR) |
| Dystonia (PNKD, GCH1, SGCE, TOR1A)
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| Fanconi-Bickel
Syndrome (SLC2A2) |
| Fingerprint
Panel |
| Fatty Acid Oxidation Disorders (ACADM, ACADS, ACADVL) |
| Fragile X Syndrome
(FMR1) |
| Galactosemia (GALT) |
| Genome Polymorphism
Scan |
| Gender Panel |
GenMax™
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Glutaric Acidemia
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Glycogen
Storage Diseases (GYS2, G6PC, SLC37A4, GAA, AGL, GBE1, PYGM, PYGL, PFKM, PHKA2, PHKA1, PHKG2 SLC2A2) |
| Greig
Cephalopolysyndactyly Syndrome (GLI3) |
| Hutchinson-Gilford Progeria (LMNA) |
| HMG-CoA Lyase Deficiency (HMGCL) |
| Isovaleric Acidemia (IVD) |
| Joubert Syndrome
(AHI1, CEP290, TMEM67/MKS3, NPHP1) |
| Laminopathies
(LMNA) |
| LEOPARD Syndrome |
| Limb Girdle Muscular Dystrophy (FCMD, FKRP, LMNA, POMT1) |
| Lymphedema
(FOXC2, FLT4) |
| Malignant
Hyperthermia (RYR1) |
| Mandibuloacral Dysplasia (LMNA, ZMPSTE24) |
| Meckel-Gruber Syndrome (MKS1, TMEM67/MKS3) |
| 3-Methylcrotonyl-CoA Carboxylase Deficiency (MCCC1, MCCC2) |
| Methylmalonic Acidemia(MUT) |
Multiminicore Disease (SEPN1) |
| Muscle-Eye-Brain Disease (POMGNT1, POMT2) |
| N-acetylglucosaminyltransferase-like Protein(LARGE) |
| NeoNatal Testing(ACADM, ACADS, ACADVL, CFTR, GALT, HMGCL, IVD, MCCC1, MCCC2, MUT, PAH, PCCA, PCCB) |
| Nephronophthisis (NPHP1) |
| Noonan Syndrome
(PTPN11, RAF1, SOS1, KRAS) |
| Organic Acidemias
(HMGCL, IVD, MCCC1, MCCC2, MUT, PCCA, PCCB) |
| Pallister-Hall Syndrome (GLI3) |
| Phenylketonuria/Phenylalanine Hydroxylase Deficiency (PAH) |
| Propionic Acidemia (PCCA, PCCB) |
| Protein O-mannose beta-1,2-N-acetylglucosaminyltransferase(POMGNT1) |
| Protein O-Mannosyltransferase 1 (POMT1) |
| Protein O-Mannosyltransferase 2 (POMT1) |
| Restrictive Dermopathy
(LMNA, ZMPSTE24) |
| SEPN1-Related Myopathies, Rigid Spine Muscular Dystrophy-1, Multiminicore Disease (SEPN1) |
| Smith-Lemli-Opitz Syndrome
(DHCR7) |
| Spondylocostal Dysostosis (DLL3, MESP2, LFNG) |
| Thrombocytopenia
(GATA1, GP1BA, GP1BB, GP9, MASTL, MPL, MYH9, RUNX1, WAS) |
| Thrombophilia
Panel (Factor V, Factor II, MTHFR) |
| Ventricular
Tachycardia (RYR2) |
| Walker-Warburg Syndrome (FCMD, FKRP, LARGE, POMGNT1, POMT1, POMT2) |
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Tests
Currently Offered By Gene
Click on the links in the following list for test descriptions, test
prices and CPT codes.
- A -
- B -
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- LAMA2 Congenital Muscular Dystrophy, Type 1A (Merosin-Deficient Congenital Muscular Dystrophy)
- LARGE N-acetylglucosaminyltransferase-like Protein
- LFNG Spondylocostal Dysostosis
- LMNA Atypical Werner Syndrome, Charcot-Marie-Tooth Neuropathy Type 2B1, Dilated Cardiomyopathy, Emery-Dreifuss Muscular Dystrophy, Familial Partial Lipodystrophy, Hutchinson-Gilford Progeria Syndrome, Lethal Tight Skin Contracture Syndrome (Restrictive Dermopathy), Limb-Girdle Muscular Dystrophy Type 1B, Lipoatrophy, LMNA-Related Dilated Cardiomyopathy, Mandibuloacral Dysplasia
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- N -
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