Genetic Counseling Genetic CounselingRelated Health News « Back to Genetic Counseling Index Sorted Alphabetically A-Z Sort by popularity 'Blond Genes' May Vary Around the World 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 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 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 Researchers Find Gene Mutations That May Be a Key to Autism Study: Gene Therapy for HIV Safe, But Effectiveness Still Unclear Your Genetic Secrets May Not Be as Safe as You Think Sorted by Popularity (as on MedicineNet) Sort alphabetically 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 45 articles 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 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: 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 Ehlers-Danlos Syndrome Ehlers-Danlos syndromes are genetic disorders that include symptoms such as loose joints, tissue weakness, easy bruising, and skin that stretches easily. Pheochromocytoma Pheochromocytoma is a tumor of the adrenal gland. Pheochromocytomas are quite rare and the vast majority of them are entirely benign. Only very rarely Sickle Cell Disease (Sickle Cell Anemia) Sickle cell anemia (sickle cell disease), a blood disease which shortens life expectancy, is cause by an inherited abnormal hemoglobin. Symptoms may include Beta Thalassemia Beta Thalassemia is the most familiar type of thalassemia. Thalassemia is not just one disease but rather a complex series of genetic (inherited) disorders 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, 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 Phenylketonuria Phenylketonuria (PKU) is a disorder that is inherited. PKU disorder increases the levels of phenylalanine in the blood. Phenylalanine is an amino acid Ramsay Hunt Syndrome Ramsay Hunt syndrome is an infection of a facial nerve that causes a red painful rash with blisters and facial paralysis. The herpes zoster virus causes Wolff-Parkinson-White Syndrome Wolff-Parkinson-White syndrome is a condition in which abnormal electrical pathways in the heart cause arrhythmias. Symptoms of Wolff-Parkinson-White syndrome Birth Defects Birth defects have many causes and currently, are the leading cause of death for infants in the first year of life. Some of the causes of birth defects 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 Achondroplasia A common form of short stature, achondroplasia (dwarfism) is a genetic condition causing a disorder of bone growth. Complications of achondroplasia that Angelman Syndrome Angelman syndrome is a genetic disorder that results from the absence of a functional copy of the UBE3A gene inherited from the mother. Infants with Angelman 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, Prader-Willi Syndrome Prader-Willi syndrome is a condition characterized by severe floppiness (hypotonia), poor growth, delayed development, and poor feeding problems in early 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 Miscarriage A miscarriage is any pregnancy that ends spontaneously before the fetus can survive. Miscarriage usually occurs before the 13th week of pregnancy. The Gilbert Syndrome Gilbert syndrome is a benign genetic condition that causes abnormal breakdown of bilirubin, a compound that is formed when hemoglobin from red blood cells Alpha Thalassemia Alpha thalassemia is a disorder in which the alpha globin protein is underproduced. There are two pairs of genes that carry the code for the alpha chains 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, 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 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, Down Syndrome Down syndrome is a genetic disorder that is caused by an additional set of chromosomes in a developing fetus. Distinctive facial features, growth retardation, Fabry Disease Fabry disease (Fabry's disease, alpha-galactosidase-A) is a genetic disorder with symptoms such as burning sensations in the hands, small-raised reddish-purplish See All Related Diseases & Conditions » Medications 0 articles Procedures & Tests 4 articles Pictures, Images & Quizzes 0 articles Doctor's & Expert's Views 4 articles Health News 21 articles Health Features 0 articles STAY INFORMED Get the latest health and medical information delivered direct to your inbox!