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A Very Special Audience: The Pope Focuses Attention on Huntington’s Disease and Rare Genetic Conditions

May 18, 2017 Dawn Laney, MS, CGC, CCRC | ThinkGenetic Co-Founder 2 Comments

Too often, due to a complex combination of fear, stigma, financial, and family implications, individuals affected by devastating rare genetic conditions like Huntington’s disease have been marginalized and misunderstood. Today,… CONTINUE

Filed Under: News Tagged With: Austedo, Dawn Jacob Laney, Dawn Laney, HD, HDSA, Huntington's disease, Huntington’s Disease Society of America, Louise Vetter, Pope Francis, Pope Francis I, Rare Disease, Rare Genetic Conditions

Weekly Site Update for 11/15/2016

November 11, 2016 thinkgenetic Leave a Comment

recently added updates

ThinkGenetic strives to create, update and review content regularly to ensure the information we provide is accurate, referenced and available 24/7 to our audience. If you wish to see your… CONTINUE

Filed Under: Updates Tagged With: adrenal cortex, Alzheimer, Alzheimer disease, ARSA, arylsulfatase A, atrophy, Beckwith-wiedemann syndrome, Bilateral renal agenesis, biotin, biotinidase, Biotinidase deficiency, birth defects, CARASIL, Choroideremia, congenital, Congenital Adrenal Hyperplasia, Cutis Laxa, dementia, DMD, Duchenne muscular dystrophy, dystroglycanopathies, EIEE2, Epileptic encephalopathy, fetal varicella syndrome, genetic disorder, GM2, HD, Hirschsprung disease, Holocarboxylase synthetase deficiency, Huntington's disease, lactase, Lactase deficiency, metabolic condition, Metachromatic leukodystrophy, MLD, Mowat-Wilson syndrome, Mucolipidosis iii alpha, Mucolipidosis iii beta, muscle disorder, muscular dystrophy, neurologic disorder, polydystrophy, Retinitis pigmentosa, Rubinstein-Taybi syndrome, seizures, strokes, Tay-sachs disease, vision, Walker-Warburg syndrome, WWS, Xeroderma pigmentosum, XP

Weekly Site Update for 09/12/2016

September 12, 2016 thinkgenetic Leave a Comment

recently added updates

ThinkGenetic strives to create, update and review content regularly to ensure the information we provide is accurate, referenced and available 24/7 to our audience. If you wish to see your… CONTINUE

Filed Under: Updates Tagged With: 2-Methyl-3-Hydroxybutryric acidemia deficiency, 2M3HBA, achondrogenesis, acromicria, ADAMTSL4, Aicardi, aicardi syndrome, alpha mannosidosis, Alpha-thalassemia, ALS, Alzheimer disease, Amyotrophic lateral sclerosis 1, and premature menopause syndrome, ARPKD, Autosomal recessive polycystic kidney disease, Barrett esophagus, CAH, CARASIL, Cartilage-hair hypoplasia, Cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy, CHH, Congenital Adrenal Hyperplasia, Congenital insensitivity to pain, Congenital lactase deficiency, Cri-du-chat syndrome, DHMN5, Dihydrolipoamide dehydrogenase deficiency, Distal hereditary motor neuropathy, DLD, eye disorder, Fabry disease, Fetal parvovirus syndrome, Fetal trimethadione syndrome, Fragile x tremor/ataxia syndrome, FXTAS, GA-1, GA-2, Gaucher disease, genetic disease, genetic disorder, Glutaric acidemia, Glutaric acidemia type 1, Glutaric acidemia type 2, HD, Hereditary Diffuse Gastric Cancer, Hereditary polyneuropathy, Huntington's disease, intellectual disability, isoleucine, Li-fraumeni syndrome, Lundberg syndrome, mental retardation syndrom, Mitochondrial Neurogastrointestinal Encephalopathy, Mucopolysaccharidosis type (MPS) IV, Muir-Torre syndrome, NBS, Nemaline Myopathy, Neuronal ceroid lipofuscinosis, Nijmegen breakage syndrome, Ornithine Transcarbamylase Deficiency, Thalidomide embryopathy, Tridione, Trisomy 20p, Trisomy 8q, type V, x-linked, X-linked juvenile retinoschisis

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