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    News and Articles on Fanconi anemia



    Toreros face Valparaiso Friday in Paradise Jam  Nov 21, 2008
    Proceeds from the activities benefited the Fanconi Anemia Research Fund and San Diego-based Father Joe's Village. For additional information, visit www. (Usdtoreros.com)

    USD Athletics Participates in First Annual Tee Off and Tip Off Fundraiser  Nov 15, 2008
    The two-day event helps the Fanconi Anemia Research Fund and San Diego-based Father Joe's Village ... Proceeds from these activities benefit the Fanconi Anemia Research Fund and San Diego-based Father Joe's Village. (Usdtoreros.com)

    Toreros open at UNLV tomorrow with 2:30 p.m. contest  Nov 15, 2008
    Proceeds from these activities benefit the Fanconi Anemia Research Fund and San Diego-based Father Joe's Village. For further information and opportunities to participate, visit www. (Usdtoreros.com)

    Storyteller gave 'wings to words'  Jul 31, 2008
    He was The Oregonian's lead writer on the Thurston High School shootings in 1998, was part of The Oregonian coverage team on the wreck of the New Carissa off the Oregon coast in 1999 and wrote a series of stories between 1991 and 1997 on the losing battles waged by Kirsten and Katie Frohnmayer with Fanconi anemia. The girls were daughters of University of Oregon president Dave Frohnmayer. (OregonLive, OR -- Sports)

    Janice Ophelia Flynt Dunham  Jul 8, 2008
    In lieu of flowers the family request that donations be made to either the First Baptist Youth Program or to the Fanconi Anemia Research Fund who can be contacted at 1-888-326-2664. Coffey~Murray Funeral Home has been entrusted to take special care of the arrangements for the Dunham family. (Durant Daily Democrat, OK)

    Researchers Pinpoint How Smoking Causes Cancer  May 15, 2008
    FANCD2 is part of a family of proteins involved in an inherited condition called Fanconi anemia. People with the condition are more likely to develop cancers at a young age and have low levels of these proteins. (Science Daily)

    The Wednesday Inside Scoop  May 2, 2008
    OregonianD ave Frohnmayer's greatest personal quest has been to find a cure for Fanconi anemia, the rare bone marrow condition that killed two daughters and now threatens a third ... Since then, the Eugene-based Fanconi Anemia Research Fund has distributed more than $10 million in research money to universities, says Mary Ellen Eiler, the group's executive director. (Oregon Sports -- Rivals.com)

    Twin Findings Raise Hopes Of Improved Anemia Treatments  Apr 17, 2008
    16, 2008) A new understanding of how red blood cell production is controlled could lead to improvements in the treatment of the blood disorder anaemia, according to West Australian medical researchers. The findings are reported in two papers published in Blood, the journal of the American Society of Hematology, by a group of Australian scientists, led by Western Australian Institute for Medical Research (WAIMR) Director Peter Klinken and his Laboratory for Cancer Medicine. (Science Daily)

    Greater Predisposition To Cancer In Those With Certain Homozygous Gene Pairs, Study Suggests  Mar 27, 2008
    30, 2008) For almost 50 years, Fanconi anemia has been associated with leukemia. Not just among those who have the genetic disorder but among their family members, whose genes, they were told, made them highly. (Science Daily)

    Parents' dilemma complex  Mar 5, 2008
    To meet him, you would never guess that in November he was diagnosed with Fanconi anemia, a rare disease that, until the advent of bone marrow transplants, killed most patients by age 12 ... Because Fanconi anemia is a genetic disease, if the Peppers go the traditional conception route, there is a one-in-four chance that the younger child would have FA, too. (News & Observer)

    America's Giving Challenge Inspires More Than 48,000 People From Around the Globe to Donate $1.2 Million Online in Just Fifty Days  Feb 21, 2008
    PARADE's America's Giving Challenge Winners: The $50,000 national winners, sponsored through Network for Good, include: -- Heidi Dormody, Boulder, CO, championed Engineers Without Borders, Inc., Longmont, CO (2979 donations, $60,655 raised, plus $50,000 award); -- Peggy Padden, Portland, OR, championed Fanconi Anemia Research Fund, Inc., Eugene, OR (2732 donations, $65,522 raised, plus $50,000 award); -- Stephen Hollister, Tustin, CA, championed IDEA League, Afton, MN (2634 donations, $62,746... (PR Newswire)

    The America's Giving Challenge and the Causes Giving Challenge Inspire More Than 80,000 People to "Give," Raising More Than $1.7 Million Online for Their Favorite Causes and Charities in Just Fifty Days  Feb 21, 2008
    -- Peggy Padden, Portland, OR, championed Fanconi Anemia Research Fund, Inc., Eugene, OR (2732 donations, $65,522 funds raised plus $50,000 award). -- Stephen Hollister, Tustin, Calif. (PR Newswire)

    Most Carriers Of Fanconi Anemia Genes Are Not At Higher Risk Of Cancer  Jan 31, 2008
    30, 2008) For almost 50 years, Fanconi anemia has been associated with leukemia ... But a new study to examine links between 13 specific Fanconi anemia genes and cancer risk has determined that in most cases, their risk of cancer is no greater than that of the rest of the population ... Fanconi anemia is primarily an autosomal recessive genetic condition, which means that in order for it to develop, a person must inherit two mutated Fanconi anemia genes, one from each parent. (Science Daily)

    Azinger given sponsor's exemption  Jan 10, 2008
    com and on eBay, with all proceeds going to designated charities, including the Fanconi Anemia Research Fund. "Having Phil involved with our charity is what we've dreamed of from the inception of Caddy For A Cure, and now having Daniel Chopra and Brett Wetterich join us for the first time is another tribute to the spirit of giving back to the community by both the players and the PGA Tour," said Russ Holden, Caddy For A Cure founder and veteran PGA Tour caddy. (AZCentral -- Sports)

    Gene Therapy Safety Trial For Childhood Blindness Under Way  Nov 20, 2007
    25, 1999) A gene therapy clinical trial for Fanconi anemia, a fatal inherited blood disease, is set to begin at the University of North Carolina at Chapel Hill. Currently, the best survival hope for Fanconi. (Science Daily)

    Balancing Act Protects Vulnerable Cells From Cancer  Nov 14, 2007
    13, 2007) Individuals who inherit one mutant copy of any one of about 12 genes that make the proteins of the Fanconi Anemia pathway are at increased risk of developing cancer. This occurs when the remaining. (Science Daily)

    U of M performs first systemic therapy for fatal childhood disease  Nov 3, 2007
    The program leads the nation in the use of umbilical cord blood in the treatment of adults and children and in the development of innovative treatments of various rare genetic diseases such as adrenoleukodystrophy (ALD) and Fanconi anemia. The transplant was done as part of a clinical trial funded by donations made to the University of Minnesota EB Fund and Childrens Cancer Research Fund in Minneapolis. (EurekAlert!)

    Memorial service honors life of Barry Simon  Oct 4, 2007
    The next afternoon, Simon, 13, died in his mother's arms after a five-year battle with a rare genetic disease for which there is no cure called Fanconi anemia. Most of the last two years were spent in Seattle in a grueling attempt to prolong Simon's life into his 20s or 30s via a bone marrow transplant. (Missoulian, MT)

    Chesapeake Child Desperately Needs Transplant  Oct 2, 2007
    Trey needs a kidney transplant which doctors were preparing him for when they made another medical discovery, Trey also suffers from a rare genetic condition called fanconi anemia, the only way to treat it is with a bone marrow transfusion. The family flew to Minnesota to see a specialist when it got even more bad news, a neighbor called last week to tell them their house had been burglarized. (WTKR.com, VA)

    Barry Simon dies in mother's arms  Sep 30, 2007
    Barry died Saturday after battling Fanconi anemia for two years ... The 13-year-old Missoula boy, who captured the hearts of hundreds of people during his two-year battle with a rare genetic disease called Fanconi anemia, died in his mother's arms at about 3 p.m.. (Missoulian, MT)

    Last goodbye: After two years in Seattle, Barry Simon comes home to die  Sep 23, 2007
    Barry was diagnosed with Fanconi anemia in 2002 and recently decided to cease medical treatment for the rare disease ... You've probably got a better chance of winning back-to-back Powerball jackpots than you do of coming down with Fanconi anemia, the rare genetic disease that is killing Barry Simon ... Only one in a million people carry the defect in a gene that causes Fanconi anemia and could be passed on to a child, and the only way to get it is for both your parents to carry the same defect.... (Missoulian, MT)

    Barry Simon coming home  Sep 2, 2007
    His doctors have told Wamsley her son, who was diagnosed with the rare and often fatal disease called Fanconi anemia at the age of 11, is not likely to live to see 2008 ... Many may have been moved to write simply because of the astronomical bad luck it takes to come down with Fanconi anemia ... The diagnosis of Fanconi anemia led to the transplant, necessary for anyone to have a chance to survive. (Missoulian, MT)

    Stem cell cure offers new hope  Jul 20, 2007
    Howard was also diagnosed with Fanconi anemia last year; a condition characterized by bone marrow failure. Today the playful eight-year-old is being presented as India's first successful case of unrelated umbilical cord blood transplantation. (NDTV.com)

    Boy fighting rare disease making stop back in town  Jun 20, 2007
    Simon's story caught the attention of many western Montanans after he was diagnosed with Fanconi anemia, a rare genetic disease that leads to bone marrow failure ... There's a one-in-a-million chance that any one person will carry the defect in an FA gene that causes Fanconi anemia, and the only way for a child to get it is for both parents to carry the same defect. (Missoulian, MT)

    Reaching maturity  Jun 8, 2007
    A year ago, Roxanne and Sergio Negrin's son, Anthony, had just been diagnosed with Fanconi anemia ... The way to the top for a children's hospital is by tackling very uncommon maladies, like Fanconi anemia, and drawing patients from all over the country, even from abroad. (Cincinnati Business Courier, OH)

    Gene Implicated In The Development Of Fanconi Anemia And Predisposition To Cancer Described  Jun 5, 2007
    An international research consortium, which included the participation of the Mutag;nesi Group from the UAB, has made progress in the study of Fanconi anaemia. They have described the function and range of possible mutations of the gene implicated in this disease that affects functions like nerve and skeletal development, blood cell formation and predisposition to cancer. (Science Daily)

    Description of a gene implicated in the development of Fanconi anemia and predisposition to cancer  Jun 2, 2007
    Public release date: 1-Jun-2007. Contact: Jordi Surralls. (EurekAlert!)

    Analysis Reveals Extent Of DNA Repair Army  May 26, 2007
    That is important, Elledge explained, because one of the big unanswered questions about BRCA1 is why it acts to suppress only some forms of cancer: The gene is "common in (all) cells, so why breast cancer and not some other kind of cancer"" Exploring the substrate domains of the ATM and ATR enzymes, Elledge added, is certain to yield deeper insight into numerous conditions mediated by faulty DNA repair mechanisms. For instance, using the new database produced by his group, Elledge and his... (Science Daily)

    Repair Of DNA By Brca2 Gene Guides Embryonic Nervous System Development, Study Suggests  May 23, 2007
    The study also gave the St. Jude researchers insights into a childhood disease called Fanconi anemia, which is caused by a mutation in the human version Brca2. Children with Fanconi anemia are at increased risk for tumors and small brain size, among other problems ... In the current study, the St. Jude team showed that mice lacking Brca2 had neurologic defects similar to those of humans with Fanconi anemia who carry the mutated gene. (Science Daily)

    Two Heads Are Better Than One: Dysfunctional DNA Repair Pathways Kill Tumor Cells  Apr 14, 2007
    Individuals who inherit two mutant copies of any one of about 12 genes that make the proteins of the Fanconi Anemia (FA) pathway develop FA, which is characterized by increased incidence of cancer and bone marrow failure, among other things. However, individuals with just a single mutant copy of one of these genes are also at increased risk of developing cancer. (Science Daily)

    * Sudanese boy with anemia waiting for marrow transplant  Mar 11, 2007
    A five-year-old Sudanese boy suffering from Fanconi Anemia experienced a pleasant Lunar New Year in central Taiwan last month thanks to the efforts of a Taiwanese woman and her Sudanese husband. The boy, Elnour Eltayeb, who has eight brothers and sisters, was diagnosed with Fanconi Anemia at the age of two. (Taipei Times, Taiwan -- World)

    Gene Elevating Breast Cancer Risk Also Causes Prostate Cancer  Feb 10, 2007
    "Present results show that the discovered PALB2 mutation elevates the risk of breast cancer four-fold. However, we still need more research to better assess the effect on cancer development. As the comprehensive mutation analysis was originally conducted on only 113 cancer families, it may be that there still are other PALB2 genetic defects accounting for heritable breast and prostate cancer susceptibility. Recent results also imply that PALB2 might be a cancer susceptibility gene in other... (Science Daily)



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