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Scientists Identify New Congenital Neutropenia Syndrome and Causative Gene Mutation A team of scientists has discovered a new syndrome associated with severe congenital neutropenia (SCN), a rare disorder in which children lack sufficient infection-fighting white cells, and identified the genetic cause of the syndrome: mutations in the gene Glucose-6-phosphatase, catalytic subunit 3 (G6PC3). TelegrapheInherited Factors Play an Important Role in Breast Cancer Progression According to New Study in Mice New research in mice and five independent collections of human breast tumors has enabled National Cancer Institute (NCI) scientists to confirm that genes for factors contributing to susceptibility for breast cancer metastasis can be inherited. TelegrapheOverview of Gum Disease Gum and periodontal disease information including photos, symptoms of gum disease, risk factors and prevention of gum disease including gingivitis and periodontitis. AboutExpanding Festive Waistlines Put Thousands At Risk Of Type 2 Diabetes Over-indulgence in too many calorific treats such as mince pies (around 200 calories each), Christmas cake (approximately 250 calories per slice) and mulled wine (about 250 calories in a glass) can leave us all struggling to buckle our belts in the New Year. Having a large waist means you are up to eleven times more likely to develop Type 2 diabetes and being overweight or obese is one of the strongest risk factors for developing Type 2 diabetes. Medicalnewstoday.comSafe New Therapy For Genetic Heart Disease A new clinical trial suggests that long-term use of candesartan, a drug currently used to treat hypertension, may significantly reduce the symptoms of genetic heart disease. The related report by Penicka et al, 'The effects of candesartan on left ventricular hypertrophy and function in non-obstructive hypertrophic cardiomyopathy: a pilot, randomized study,' appears in the January issue of The Journal of Molecular Diagnostics. Medical News TodayGenetic Variation In Young Heart Attack Patients Results In Anticlotting Drug Clopidogrel Being Less Effective If a young heart attack patient (under 45 years of age) has a certain genetic variation, the anticlotting drug clopidogrel is less effective in that person and they are much more likely to die, have another heart attack, require urgent repeat coronary intervention or have stent thrombosis. Medical News TodayScientists Identify New Congenital Neutropenia Syndrome And Causative Gene Mutation Scientists have discovered a new syndrome associated with severe congenital neutropenia, a rare disorder in which children lack sufficient infection-fighting white cells, and identified the genetic cause of the syndrome. MedicineNetGenetic variation may lead to early cardiovascular disease (Public Library of Science) Researchers from Duke University Medical Center have identified a variation in a particular gene that increases susceptibility to early coronary artery disease. For years, scientists have known that the devastating, early-onset form of the disease was inherited, but they knew little about the gene(s) responsible until now. The results are published Jan. 2 in the open-access journal PLoS Genetics. CBC.ca |
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