Why Choose Berries Health DNA Screening?

– 🧬 Analyzes over 20,000 genes
– 💡 Identifies causes of chronic, inherited, or rare conditions
– Covering more than 6,800 rare diseases
– 🧓 Ideal for seniors and families with a history of illness
– 🔍 Detects risks for diseases like Alzheimer’s, inherited cancers, diabetes, and joint disorders (see details at the bottom of the page)
– No physician referral needed
– 🛡 HIPAA-compliant and fully confidential
– 👨‍⚕ Free genetic counseling with expert board certified counselors available before and after the test

Is This Test Right for You?

– ❓ Struggling with a chronic condition of unknown cause?
– 👪 Have a family history of serious illnesses?
– .🌱 Want to proactively manage your health and future?
➡ Then this test is a great fit for you.

Limited Time Offer – $1,799 Only!

This comprehensive genetic screening is typically offered through high-end concierge services or specialized clinics. Take advantage of this special rate today.

Overview of Genetic Risk Factors for Various Diseases

This document aims to outline the potential genetic risks associated with several diseases, spanning various categories. Understanding these risks can provide valuable insights for early detection and management.

Neurodegenerative Diseases

• Early-Onset Alzheimer’s Disease: A genetic predisposition that may lead to an earlier onset of Alzheimer’s symptoms.
• Familial Parkinson’s Disease: Inherited forms of Parkinson’s that can significantly affect movement and coordination.
• Frontotemporal Dementia (FTD): A group of disorders caused by progressive degeneration of the frontal and temporal lobes of the brain.
• Amyotrophic Lateral Sclerosis (ALS): A fatal condition affecting nerve cells in the brain and spinal cord, often with hereditary links.
• Spinocerebellar Ataxias: A group of genetic disorders characterized by degeneration of the cerebellum, leading to coordination issues.

Cardiometabolic Disorders

• Familial Hypercholesterolemia: A genetic condition that leads to high cholesterol levels, increasing heart disease risk.
• Familial Combined Hyperlipidemia: An inherited disorder that results in high levels of cholesterol and triglycerides.
• Familial Hypertriglyceridemia: A genetic predisposition to elevated triglyceride levels in the blood.
• Tangier Disease: A rare genetic disorder affecting cholesterol metabolism.

Ophthalmologic Disorders

• Adult-Onset Retinitis Pigmentosa: A genetic condition leading to progressive vision loss, typically starting in adulthood.
• Hereditary Glaucoma (Adult Form): A genetic risk factor for increased intraocular pressure and potential vision loss.
• Monogenic Macular Degeneration: A genetic condition that can lead to vision impairment due to degeneration of the macula.

Skeletal/Bone Disorders

• Paget’s Disease of Bone: A disorder that disrupts the normal recycling process of bone tissue, potentially leading to deformities.
• Adult-Onset Hypophosphatasia: A genetic condition affecting bone mineralization.
• Adult-Onset Osteopetrosis: A rare bone disease characterized by the abnormal density of bones.

Endocrine Disorders

• Multiple Endocrine Neoplasia (MEN1, MEN2): Genetic syndromes that cause tumors in endocrine glands.
• Hereditary Hemochromatosis: A condition causing excessive iron absorption and deposition in the body.
• Autoimmune Polyendocrine Syndrome (APS-2): A genetic disorder leading to multiple autoimmune issues affecting endocrine glands.

Metabolic/Diabetes Disorders

• MODY (Maturity Onset Diabetes of the Young): A form of diabetes caused by a genetic mutation, diagnosed typically in adults.
• Familial Partial Lipodystrophy: A condition characterized by abnormal fat distribution in the body.

Cancer Syndromes

• BRCA1/2-Associated Breast & Ovarian Cancer: Genetic mutations that significantly increase the risk of breast and ovarian cancers.
• Colorectal cancer: An inherited condition that increases the risk of various cancers, especially colorectal cancer.
• Li-Fraumeni Syndrome: A genetic disorder that predisposes individuals to a variety of cancers.

Other Genetic Disorders

• Hereditary Amyloidosis: A condition where abnormal protein deposits affect organs and tissues.
• Alpha-1 Antitrypsin Deficiency: A genetic disorder that can lead to lung and liver disease.
• Gitelman Syndrome (Adult-Diagnosed): A genetic disorder affecting the kidneys and leading to electrolyte imbalances.
• Hereditary Angioedema (Non-Pediatric Forms): A genetic condition that causes severe swelling episodes.