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April Book Spotlight: “Can I Play if I Have Fabry?” by Dawn Laney

April 8, 2021 Jessica Dronen, MS, CGC 1 Comment

by Jessica Dronen, MS, CGC, Genetic Diseases Research and Information Specialist, ThinkGenetic Welcome to ThinkGenetic’s first genetic book spotlight! Starting this month we will be pairing a review of one… CONTINUE

Filed Under: Education, Genetic Book Club Tagged With: book club, Can I Play if I Have Fabry, childrens book, Dawn Jacob, Dawn Jacob Laney, Fabry, Fabry disease, Fabry Support and Information Group, FSIG, Jessica Dronen, National Fabry Disease Foundation, NFDF

Speakers Announced – Lafayette Lunch and Learn

May 30, 2019 Ruth O'Keefe Leave a Comment

The ThinkGenetic Foundation is very excited to announce the confirmed Speakers and Patient Panelists for the upcoming FREE Lunch and Learn:Closing the Genetics Gap: A Discussion on Increasing Education and… CONTINUE

Filed Under: Advocacy, Education, Events, Lafayette Tagged With: Acadiana, Annie Arabie, Carol Ogg, Cynthia Bordelon Durham, Dan Arabie, Dawn Laney, Fabry, FARA, friedreich's ataxia, FSIG, Lafayette, Lafayette General Health, Louisiana, Lunch and Learn, Margaret Landry-Bearb, Matthew Lafleur, NFDF, Robin Richardson, Sanofi Genzyme, ThinkGenetic, ThinkGenetic Foundation, usher, Usher Syndrome Coalition

Canadian Fabry Association Partners with ThinkGenetic To Broaden Support for Patients with Fabry Disease

October 18, 2017 Ruth O'Keefe Leave a Comment

The Canadian Fabry Association (CFA), a non-profit organization raising awareness and educating the public about Fabry disease, has joined ThinkGenetic’s Advocacy Partner program. The CFA is committed to improving the… CONTINUE

Filed Under: Partners Tagged With: advocacy partner, Canadian Fabry Association, CFA, Fabry, Julia Alton, Len Barker, partnership

Partnership in the FDNA Year of Discovery

May 15, 2017 Carol Ogg, BS Pharm 2 Comments

   Not too long ago it was taught in medical school that rare diseases were just that- rare and you probably wouldn’t see a patient with a rare disease in… CONTINUE

Filed Under: Education, Partners Tagged With: Carol Ogg, Fabry, Fabry disease, Face2Gene, Facial Phenotypes, FDNA, Homocystinuria, IEM, inborn errors of metabolism, inherited metablic disorder, LSD, lysosomal storage diseases, metabolic conditions, MPS Diseases, Mucopolysaccharidosis, Rare Disease, Year of Discovery

Site Update for Week of 12/01/2016

December 1, 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 anyone searching for answers on genetic diseases and… CONTINUE

Filed Under: Updates Tagged With: Acromegaly, Acyl-coa dehydrogenase, ADAMTSL4, Agammaglobulinemia, Alagille syndrome, Alkaptonuria, Campomelic dysplasia, Cartilage-hair hypoplasia, Ceroid lipofuscinosis, CHARGE syndrome, chromosome pairs, congenital heart defect, developmental delay, DNA, enzyme, Fabry, Gal-1-PUT, galactose-1-phosphate uridyl transferase, Galactosemia, gene, genetic condition, glucose, Glutaric acidemia, glycogen storage disease, growth hormone, Huntington, hypogonadotropic hypogonadism, Kallman syndrome, Leopard syndrome, Mosaic trisomy 14, Noonan syndrome, Otosclerosis, Pitt-Hopkins syndrome, pituitary gland, protein, PTHS, Rare Disease, rare genetic disorder, Rett syndrome, Robinow syndrome, Sandhoff disease, Sickle cell anemia, Spinal muscular atrophy, Stickler syndrome, sugar, SYNGAP1, triple X syndrome, Trisomy 13, Trisomy x, webbed neck, XXX

Weekly Site Update for 09/19/2016

September 19, 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: Achondroplasia, dwarfism, Fabry, Fabry disease

6th Annual Fabry Family Medical Conference

September 6, 2016 Ruth O'Keefe Leave a Comment

Featured - NFDF

On September 8-9, 2016 in Greensboro, North Carolina the National Fabry Disease Foundation (NFDF) will be hosting it’s annual Fabry Family Medical Conference. An important event for all individuals with Fabry disease… CONTINUE

Filed Under: Events, News Tagged With: Dave Jacob, Dawn Laney, Emory University, Fabry, Fabry disease, Fabry Family Medical Conference, genetic counselor, National Fabry Disease Foundation, NFDF, Ruth O'Keefe

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