{"id":106623,"date":"2014-02-06T17:42:40","date_gmt":"2014-02-06T22:42:40","guid":{"rendered":"http:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/uncategorized\/to-catch-a-killer-gene-sisters-race-to-stop-mystery-disease.php"},"modified":"2014-02-06T17:42:40","modified_gmt":"2014-02-06T22:42:40","slug":"to-catch-a-killer-gene-sisters-race-to-stop-mystery-disease","status":"publish","type":"post","link":"https:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/eugenics\/to-catch-a-killer-gene-sisters-race-to-stop-mystery-disease.php","title":{"rendered":"To Catch a Killer Gene: Sisters Race to Stop Mystery Disease"},"content":{"rendered":"<p><p>    Days before she ended her pregnancy,    Joselin Linder was thrilled to imagine herself as a parent. She    was 37, newly-married, and though her baby-to-be wasnt    planned, it was soon deeply desired. Maybe its that I played    with dolls until I was so old I had to play with them in my    closet, she says. But it seemed inevitable that I would one    day be a mother.  <\/p>\n<p>    Linder is not a mother today, more than a    year later, because she had an abortion at 10 weeks. She still    wanted the childwanted to call it George, perhapsbut she    feared she would pass along the disease that killed her father    in mid-life, practically fusing his organs and ballooning his    body. She and her sister Hilary inherited the same unnamed    illness, but as with most of the thousands of inheritable    diseases known to science, there is no cureexcept for stopping    the affected bloodline.  <\/p>\n<p>    Its an agonizing form of prevention the    Linder sisters have turned to four times combined. Theyve had    three abortions, and in 2009, Hilary and her husband paid    $20,000 out of pocket for a round of in vitro fertilization    aimed at creating an unaffected embryo. The gene has killed    five people in the Linder family, and it now threatens the    sisters themselves. But if they have their way, it will die out    in their generation.  <\/p>\n<p>    I think thats a big deal, says Joselin,    who lives in Brooklyn, N.Y. I think weve done something    amazing with this particular gene.  <\/p>\n<p>    The Linders story is personal, of course,    but its also a public milestone. Its the first known example    of genetic medicine not only identifying a deadly new    mutationakin to the next Huntingtons or Cystic Fibrosisbut    of a family banding together to stop a disease before it cuts a    path through society itself. It illustrates the promise of    genomic medicine, which may one day stop disease as we know it,    but also the soul-troubling questions that arise when people    have a hand in their own evolution.  <\/p>\n<p>    America is experiencing a boom in    biological fortune-telling. Doctors can now scan the genes of a    fetus using only a drop of the mothers blood, testing for    hundreds of known mutations, including Down syndrome. Soon    theyll be able to detect a growing list of rare    mutationsalmost none of them treatableand predict an embryos    risk of more common ailments like diabetes, cancer, and heart    disease. By that point, millions of pregnant women will be    offered a God-like view of their child-to-be and a decision    much like the Linders, a decision as miraculous as it is    unnerving: When is a life worth living?  <\/p>\n<p>    The family gene, as Joselin calls it, surfaced in the    late 1980s, when her father William came home from a family    trip complaining of swollen legs and strange fatigue. He waved    it off as jet lag, but the swelling spread and the fatigue    deepened. He was 40, vibrant and fit, a busy doctor in    Columbus, Ohio. But within a couple years he was forced into    semi-retirement, hardly able to take the stairs.  <\/p>\n<p>    Im very, very sick, he told Joselin, who    was then 17, and surprised to see her father start to cry. In    the years that followed, his body filled with a creamy white    fluid, which doctors pumped out by the liter. He got rounder,    but lighter, his muscles withering even as something in his    belly grew.  <\/p>\n<p>    He moved into Brigham and Womens Hospital,    a Harvard-affiliated facility in Boston, where he confounded    some of the countrys best doctors. In his records, which    Joselin shared with NBC News, a series of gobsmacked    specialists noted puzzling resultsan occult    malignancysomething brewing. None could come up with a    diagnosis, however, let alone a cure.  <\/p>\n<p>    William Linder died a medical mystery in    September of 1996, his autopsy revealing a body both starved    and bloated. The cause of death was officially unknown. His    daughters visited him often, right to the end, shuffling ICU    visits into their college schedules. They never suspected that    they were getting a preview of their own genetic    destiny.  <\/p>\n<p><!-- Auto Generated --><\/p>\n<p>Read the original here:<\/p>\n<p><a target=\"_blank\" href=\"http:\/\/feeds.nbcnews.com\/c\/35002\/f\/663303\/s\/36c722c2\/sc\/38\/l\/0L0Snbcnews0N0Cnews0Cus0Enews0Ccatch0Ekiller0Egene0Esisters0Erace0Estop0Emystery0Edisease0En14451\/story01.htm\" title=\"To Catch a Killer Gene: Sisters Race to Stop Mystery Disease\">To Catch a Killer Gene: Sisters Race to Stop Mystery Disease<\/a><\/p>\n","protected":false},"excerpt":{"rendered":"<p> Days before she ended her pregnancy, Joselin Linder was thrilled to imagine herself as a parent. She was 37, newly-married, and though her baby-to-be wasnt planned, it was soon deeply desired <a href=\"https:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/eugenics\/to-catch-a-killer-gene-sisters-race-to-stop-mystery-disease.php\">Continue reading <span class=\"meta-nav\">&rarr;<\/span><\/a><\/p>\n","protected":false},"author":1,"featured_media":0,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":{"limit_modified_date":"","last_modified_date":"","_lmt_disableupdate":"","_lmt_disable":"","footnotes":""},"categories":[23],"tags":[],"class_list":["post-106623","post","type-post","status-publish","format-standard","hentry","category-eugenics"],"modified_by":null,"_links":{"self":[{"href":"https:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/wp-json\/wp\/v2\/posts\/106623"}],"collection":[{"href":"https:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"https:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"https:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/wp-json\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"https:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/wp-json\/wp\/v2\/comments?post=106623"}],"version-history":[{"count":0,"href":"https:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/wp-json\/wp\/v2\/posts\/106623\/revisions"}],"wp:attachment":[{"href":"https:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/wp-json\/wp\/v2\/media?parent=106623"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/wp-json\/wp\/v2\/categories?post=106623"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/wp-json\/wp\/v2\/tags?post=106623"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}