Genetic Counseling Genetic CounselingRelated Health News « Back to Genetic Counseling Index Sorted Alphabetically A-Z Sort by popularity 'Angelina Jolie Effect' Prompted More Testing for Breast Cancer Genes: Study 'Blond Genes' May Vary Around the World 6 in 10 Americans Interested in Genetic Testing, Survey Finds Better-Informed Women Order Fewer Prenatal Gene Tests, Study Finds Bonobo Genome Sheds Light on Their Links to Chimps, Humans Brave New World of Genetics Requires Safeguards, Experts Say Carriers of Breast Cancer Gene at Risk of Second Cancer Concerns Raised About Drugstore Genetic Test Discovery of 100-Plus Genes Tied to Autism May Improve Treatments Family Members of Kids With Cancer Also at Risk Gene Mapping for Healthy People No 'Crystal Ball' Gene Studies Support 'Queen of Sheba' Legend Gene Tests May Not Drive Patients to More Medical Care Gene Therapy Shows Promise for Rare Immune Disorder Genetic Disorder Test for Newborns May Speed Up Diagnoses Genetic Research Sheds Light on Jewish Diaspora Genetic Test May Spot Raised Autism Risk Health Highlights: Feb. 3, 2012 Healthier Lifestyle After at-Home Genetic Test? Many Black Women Prone to Gene-Driven Breast Cancer: Study Most Americans Want Doctors' Help With Gene Test Results: Study New Clues on Genetic Causes of Autism Obesity Gene Tests May Not Hamper Weight-Loss Efforts Parents of a Child With Autism Often Forgo Further Childbearing: Study Phone Counseling Helps Rural Women With Cancer Gene Tests Researchers Find Gene Mutations That May Be a Key to Autism Study: Gene Therapy for HIV Safe, But Effectiveness Still Unclear Whole-Genome Scans Not Quite Ready for Widespread Use: Study Your Genetic Secrets May Not Be as Safe as You Think Sorted by Popularity (as on MedicineNet) Sort alphabetically Gene Therapy Shows Promise for Rare Immune Disorder 6 in 10 Americans Interested in Genetic Testing, Survey Finds Phone Counseling Helps Rural Women With Cancer Gene Tests Discovery of 100-Plus Genes Tied to Autism May Improve Treatments Better-Informed Women Order Fewer Prenatal Gene Tests, Study Finds 'Angelina Jolie Effect' Prompted More Testing for Breast Cancer Genes: Study Parents of a Child With Autism Often Forgo Further Childbearing: Study Whole-Genome Scans Not Quite Ready for Widespread Use: Study Most Americans Want Doctors' Help With Gene Test Results: Study Obesity Gene Tests May Not Hamper Weight-Loss Efforts Family Members of Kids With Cancer Also at Risk Many Black Women Prone to Gene-Driven Breast Cancer: Study Your Genetic Secrets May Not Be as Safe as You Think Genetic Disorder Test for Newborns May Speed Up Diagnoses Genetic Research Sheds Light on Jewish Diaspora Gene Studies Support 'Queen of Sheba' Legend Bonobo Genome Sheds Light on Their Links to Chimps, Humans Brave New World of Genetics Requires Safeguards, Experts Say Gene Tests May Not Drive Patients to More Medical Care Genetic Test May Spot Raised Autism Risk 'Blond Genes' May Vary Around the World Study: Gene Therapy for HIV Safe, But Effectiveness Still Unclear Researchers Find Gene Mutations That May Be a Key to Autism Gene Mapping for Healthy People No 'Crystal Ball' Health Highlights: Feb. 3, 2012 Carriers of Breast Cancer Gene at Risk of Second Cancer New Clues on Genetic Causes of Autism Healthier Lifestyle After at-Home Genetic Test? Concerns Raised About Drugstore Genetic Test Suggested Reading on Genetic Counseling by Our Doctors Related Diseases & Conditions 48 articles Campomelic Dysplasia Campomelic dysplasia is a rare inherited condition that may be life threatening. The condition affects the skeleton and reproductive system. Rothmund-Thomson Syndrome Rothmund-Thomson syndrome is a rare genetic. The signs and symptoms of Rothmund-Thomson syndrome include a redness on the cheeks (developed between the Pycnodysostosis Pycnodysostosis (pyknodysostosis) is an inherited disease of the bone. Characteristics of individuals with pycnodysostosis are short stature, brittle bones, Gaucher Disease Gaucher disease is caused by an inherited (genetic) defect in an enzyme glucocerebroside. Signs fo Gaucher disease include enlargement of the spleen, fatique, Pregnancy Planning Pregnancy planning is an important step in preparation for starting or expanding a family. Planning for a pregnancy includes taking prenatal vitamins, Williams Syndrome Williams syndrome is a developmental disorder that affects many parts of the body. Features may include intellectual disability, learning problems, unique Porphyria Porphyria is a group of disorders that affect the nervous system, skin, or both. Porphyria is often an inherited condition that causes blistering, itching, Face Blindness (Prosopagnosia) Face blindness (prosopagnosia) is a condition that causes the inability to recognize faces. Face blindness may be caused by stroke, traumatic brain injury, Treacher Collins Syndrome Treacher Collins syndrome is a rare genetic condition that affects the development of the bones and tissues of the face. Symptoms can range from mild to Kidney Dysplasia Kidney dysplasia is a condition in which one or both of a baby's kidneys do not develop normally. In kidney dysplasia, cysts replace normal kidney tissue. Hemochromatosis (Iron Overload) Hereditary hemochromatosis (iron overload) is an inherited disorder in which there is excessive accumulation of iron in the body. Individuals may have Huntington's Disease Huntington's disease is the result of degeneration of neurons in areas of the brain. Huntington's disease is an inherited disorder. Early symptoms include Marfan Syndrome Marfan syndrome is hereditary condition affecting connective tissue. A person with Marfan syndrome may exhibit the following symptoms and characteristics: Miscarriage Miscarriage is the medical term for the spontaneous loss of pregnancy from conception to 20 weeks gestation. Risk factors for a woman having a miscarriage Pick Disease Frontotemporal dementia (FTD) is a syndrome that is associated with shrinking of the frontal and temporal lobes of the brain. Frontotemporal dementia used Achondroplasia A common form of short stature, achondroplasia (dwarfism) is a genetic condition causing a disorder of bone growth. Complications of achondroplasia that Amyotrophic Lateral Sclerosis (ALS) Amyotrophic lateral sclerosis (ALS, Lou Gehrig's disease) is a neurological disease that progresses rapidly. The disease attacks the nerve cells responsible Alpha-1 Antitrypsin Deficiency Alpha-1 antitrypsin deficiency is an inherited disorder that may cause liver and lung disease in adults. Signs and symptoms include shortness of breath, Breast Cancer Breast cancer is an invasive tumor that develops in the mammary gland. Breast cancer is detected via mammograms, breast self-examination (BSE), biopsy, Colon Cancer Colon cancer is a malignancy that arises from the inner lining of the colon. Most, if not all, of these cancers develop from colonic polyps. Removal of Canavan Disease Canavan disease is an inherited genetic disorder that typically causes death before 10 years of age. Signs and symptoms of the disease include developmental Cerebral Palsy Cerebral palsy (CP) is an abnormality of motor function and postural tone acquired at an early age (even before birth). Cerebral palsy is generally caused Usher Syndrome There are three types of Usher (Usher's) syndrome, the most common condition that affects both vision and hearing. The major symptoms of Usher syndrome Colon Cancer Prevention Colo-rectal cancer is both curable and preventable if it is detected early and completely removed before the cancerous cells metastasize to other parts Genetic Disease Genetic disease is a disorder or condition caused by abnormalities in a person's genome. Types of genetic inheritance include single inheritance (for example, Charcot-Marie-Tooth-Disease Charcot-Marie-Tooth disease is one of the most common inherited neurological disorders. Charcot-Marie-Tooth disease affects the peripheral nerves. Symptoms Loeys-Dietz Syndrome Loeys-Dietz syndrome is a syndrome is an inherited genetic syndrome characterized by aortic aneurysms in children. Children with Loeys-Dietz syndrome are Fragile X Syndrome Fragile X syndrome is the most common inherited form of mental retardation. It's caused by a mutation on the X chromosome. People with Fragile X syndrome Prader-Willi Syndrome Prader-Willi syndrome is a condition characterized by severe floppiness (hypotonia), poor growth, delayed development, and poor feeding problems in early See All Related Diseases & Conditions » Medications 0 articles Procedures & Tests 5 articles Pictures, Images & Quizzes 0 articles Doctor's & Expert's Views 4 articles Health News 29 articles Health Features 0 articles STAY INFORMED Get the latest health and medical information delivered direct to your inbox!