21. Fanconi Anemia, Cincinnati Childrens Hospital Medical Center What is Known about fanconi anemia. fanconi anemia (FA) is one of the inheritedanemias that leads to bone marrow failure, or aplastic anemia. http://www.cincinnatichildrens.org/Health_Topics/Your_Childs_Health/Hematology_a

Your Child's Health Hematology and Blood Overview Conditions and Diagnoses ... Hematology and Blood Disorders Fanconi Anemia Sickle Cell Anemia Tests and Procedures Home Care Conditions and Diagnoses Fanconi Anemia: Signs, Symptoms, Long-Term Outlook Fanconi Anemia (FA) is one of the inherited anemias that leads to bone marrow failure or aplastic anemia. Fanconi Anemia is an autosomal recessive disorder. If both parents carry a defect (mutation) in the same Fanconi Anemia gene, and if their children inherit the defective gene from both parents, the child will be born with Fanconi Anemia. Signs and Symptoms Fanconi Anemia may be evident at birth by a combination of the following physical traits: Short stature Thumb, arm, and skeletal anomalies in the hips, spine, and ribs Kidney problems Skin discoloration Small head and eyes Learning disabilities Low birth weight Gastrointestinal difficulties Small reproductive organs in males Heart defects Children with Fanconi Anemia are usually diagnosed by age 12, when they may exhibit some or all of these symptoms: Sudden and extreme fatigue Recurrent infections Frequent nosebleeds Easy bruising Long-Term Outlook Fanconi Anemia usually becomes more severe over time. There is also a risk that some patients may develop leukemia or other cancers.

22. Hope For Henry This web site is dedicated to helping people learn more about what a special young man Henry is and to educate everyone about the disease he is fighting, fanconi anemia. http://www.hsg.org/

Read the N.Y. Times.com article about Henry! Publish Date June 30, 2001 Henry Strongin Goldberg was born on October 25, 1995. Henry knows all there is to know about Pokémon, believes that Disney World is the best place on earth, plays soccer, worships superheroes and wrestles with his younger brother Jack way past bedtime. Everything he does makes his parents smile. In these and so many other ways, Henry is a lot like other boys his age. But this lover of life and everything Batman is different from other kids because Henry has a horrible disease that threatens his life. After a scary and difficult five years of endless waiting rooms, doctor's visits, blood tests, EKG's, bone marrow aspirations, IV's, surgeries, transfusions, drugs, scars and a bone marrow transplant in July 2000 that met with innumerable complications, Henry faces a very uncertain future. This web site is dedicated to helping people learn more about what a special and brave young man Henry is and to educate everyone about the disease he is fighting, Fanconi anemia (FA). Through raising awareness and money for research and encouraging people to register to be a bone marrow donor, our family strives to give Hope for Henry and other children suffering from this killer. We welcome you to the site and encourage you to tell others about it and to bookmark this page so you can keep abreast of Henry's progress.

23. Fanconi Anemia Comprehensive Care Center, Cincinnati Childrens Hospital Medical fanconi anemia. Overview Together, Dr. Harris and Dr. Williams are leading a teamof caring experts at the first multidisciplinary fanconi anemia care center. http://www.cincinnatichildrens.org/Services/Programs_And_Services/Fanconi_Anemia

Services / Programs Overview Related Resources Contact Us Faculty and Staff Fanconi Anemia Comprehensive Care Center Overview Find Other Related Hematology/Oncology Programs and Services New Approach to Care, Renewed Hope for Patients and Families The Fanconi Anemia Comprehensive Care Center at Cincinnati Children's Hospital Medical Center is a first-of-its-kind center in the United States dedicated to compassionate, multidisciplinary care of children with Fanconi Anemia (FA) and other rare bone marrow failure syndromes. Distinguished experts Richard Harris, MD , and David Williams, MD , lead a team of specialists to deliver organized, outstanding medical, surgical and behavioral care at multiple levels. At the Fanconi Anemia Comprehensive Care Center, you'll discover a unique focus on care for children with Fanconi Anemia and support for their families. Multidisciplinary Approach Offers Patients Optimal Care The Fanconi Anemia Comprehensive Care Center provides a multidisciplinary approach to caring for children with Fanconi Anemia and other rare bone marrow failure syndromes. Collectively, experts from numerous areas of specialty can offer children and their families optimal care. The Fanconi Anemia Comprehensive Care Center designs personalized, ongoing treatment regimens for patients, delivered by specialists in the following areas:

24. Fanconi Anemia: The Frohnmayer Family's Experience The personal story of David and Lynn Frohnmayer whose three daughters were born with fanconi anemia, an inherited, usually fatal illness. http://darkwing.uoregon.edu/~lfrohn/

25. Fanconi Anemia: The Frohnmayer Family's Experience http://oregon.uoregon.edu/~lfrohn/lynn.html

26. WELCOME TO FANCONI CANADA Canadian charity whose mission is to fund medical research into finding a cure for fanconi anemia and to serve as a support network for affected Canadian families. http://www.fanconicanada.org

FANCONI CANADA Home Fanconi Anemia About Fanconi Canada FA News You Can Help FA Worldwide Canadian Faces of FA Contact Us ... Family Websites FAMILIES Family Welcome Page PHYSICIANS/RESEARCHERS Sitemap Home Virtual Office of GIVE THEM TOMORROW Welcome to the home of Fanconi Canada on the world wide web. OUR MISSION Fanconi Canada is a registered charity whose mission is to fund research in Canada into an effective treatment and, ultimately, a cure for Fanconi Anemia and to serve as a support network for affected Canadian families. Canada Customs and Revenue Agency registration no. 868951724 RR 0001 (formerly 890840549 RR 0001) Thanks for Visiting! Canadian Fanconi Anemia Research Fund / La Fondation Canadienne de Recherche de L'Anemie de Fanconi Home Fanconi Anemia About Fanconi Canada FA News You Can Help FA Worldwide Canadian Faces of FA Contact Us ... Family Welcome Page

27. BMT InfoNet Home Page Breast Cancer. Cancer general. fanconi anemia. Graft-Versus-Host Disease. GriefCounselling. Immune Deficiency. Becoming a Donor. Finding a Donor. fanconi anemia. http://www2.bmtnews.org/resource/index.cfm?Fuseaction=ResourceResults&Category=2

28. B+ Home A charitable organization providing assistance to children with fanconi anemia within the St. Louis and St. Charles Missouri metro areas. http://www.bpositiveinc.com

B Positive! Bone Marrow Drive Schedule UPDATE B Positive, Inc. P.O. Box 533 Chesterfield, Mo. 63006-0533 (314) 503-BPOS (2767) In December, 2000, two St. Louis area siblings, Matthew Pearl, age 4, and Alexandra Pearl, age 6, were diagnosed with Fanconi Anemia . At the same time, they discovered that each child had B+ blood types and that their only hope for finding a cure was successful bone marrow transplant. The odds of any given individual, other than an immediate family member, being a perfect match is about one in a million. Alex received her bone marrow transplant in May, 2001 and is recovering well... however, no match for Matt has been found yet. We need your help! For more about Alex and Matt, visit their web site at www.alexandmatt.com Welcome to the B Positive, Inc. Web Site! NEW UPCOMING EVENTS! Bone Marrow Drive Schedule UPDATE Matthew, Oct. 4, 2002 at the 2nd Annual B Positive Dinner/Auction Dear Friends, CLICK HERE TO SEE PHOTOS OF ALL THE FESTIVITIES! For those who do not know exactly what Fanconi Anemia is, it is a genetic, life-threatening, inherited blood disorder that leads to bone marrow failure. It occurs equally in males and females and is found in all ethnic groups. Though considered primarily a blood disorder, it may affect all systems of the body. Many patients develop acute myelgenous leukemia (AML). Older patients may develop other cancers. Many patients will not reach adulthood. Currently the only long-term cure for Fanconi Anemia is a bone marrow transplant. For additional information, please refer to

29. Aplastic Anemia fanconi anemia Fanconi's Anemia. Page, Marrow Index. http://www.fpnotebook.com/HEM132.htm

Home About Links Index ... Editor's Choice Paid Advertisement (click above). Please see the privacy statement Hematology and Oncology Marrow Anemia Aplastic Anemia Fanconi Anemia Assorted Pages Macroglobulinemia Multiple Myeloma Myelofibrosis Polycythemia Rubra Vera ... Bone Marrow Aspiration Aplastic Anemia Book Home Page Cardiovascular Medicine Dental Dermatology Emergency Medicine Endocrinology Gastroenterology General Medicine Geriatric Medicine Gynecology Hematology and Oncology HIV Infectious Disease Jokes Laboratory Neonatology Nephrology Neurology Obstetrics Ophthalmology Orthopedics Otolaryngology Pediatrics Pharmacology Prevention Psychiatry Pulmonology Radiology Rheumatology Sports Medicine Surgery Urology Chapter Hematology and Oncology Index Anemia Cancer Coagulopathy Cardiovascular Medicine Dermatology Endocrinology Otolaryngology Examination Gastroenterology Hematology and Oncology Hemoglobin Hemolysis Histiocytosis HIV Infectious Disease Laboratory Leukemia General Pulmonology Lymph Marrow Neurology Obstetrics Orthopedics Pediatrics Pharmacology Platelet Prevention Procedure Psychiatry Rheumatology Surgery Symptom Evaluation Vascular Page Marrow Index Anemia Aplastic Anemia Fanconi Macroglobulinemia Multiple Myeloma Myelofibrosis Polycythemia Epidemiology Median age of onset: 25 years Presentation: Symptoms Fatigue Fever Causes: Acquired Idiopathic (most common cause) Viral infection Infectious Mononucleosis Viral Hepatitis (non-A non-B non-C) Human Immunodeficiency Virus Medications Cancer Chemotherapy (common cause) Antileukemic medications Nitrogen mustard

30. Alex And Matt Pearl Personal stories of two children fighting fanconi anemia. http://www.alexandmatt.com

photos - (click here) Hi, most of you may know our story; we are Alexandra and Matthew Pearl. In December 2000 and January 2001 we were both diagnosed with a rare, life threatening blood disease called Fanconi anemia. It causes bone marrow failure; our bodies cannot make the blood we need to survive. Our only hope is a bone marrow transplant. Alex has found a perfect match and is recovering from her May 31, 2001 transplant in Cincinnati, Ohio. There is no perfect match for Matthew, in any registry throughout the entire world. We need your help, please consider getting added to the National Bone Marrow Registry through the Pearl Million-Donor March. Refer to the ' How You Can Help ' section. Pearl Family Million Donor March Presentation (PPT) My little girl (PPT) ... more docs, click here Who knows, maybe you could be the perfect match that saves Matthew's or the 3,000 others in need. Thanks to all who have helped to add more than 17,000 people to the registry, that have resulted in at least 40 matches for others. It is a good start, but there is much work to be done. God Bless and Thank you

31. Kprones FA10001 Karyotype evolution in the bone marrow of a patient with fanconi anemia breakpointsin clonal anomalies of this disease. fanconi anemia and DNA repair. http://www.infobiogen.fr/services/chromcancer/Kprones/FA10001.html

Atlas of Genetics and Cytogenetics in Oncology and Haematology Home Genes Leukemias Solid Tumours ... NA Fanconi anaemia Identity Note Fanconi anaemia is a chromosome instability syndrome with progressive bone marrow failure and an increased risk of cancers Other names Fanconi pancytopenia Inheritance autosomal recessive; frequency is about 2.5/10 newborns Clinics Phenotype and clinics growth retardation (70% of cases) skin abnormalities: hyperpigmentation and/or café au lait spots in 80% squeletal malformations (60%), particularly radius axis defects (absent or hypoplastic thumb or radius...) no immune deficiency (in contrast with most other chromosome instability syndromes) progressive bone marrow failure; mean age of onset of anemia: 8 yrs; diagnosis made before onset of haematologic manifestations in only 30% other: renal anomalies, hypogonadism, mental impairment, heart defects, and perhaps diabetes mellitus, also occur in 10 to 30% of cases Neoplastic risk myelodysplasia (MDS) and acute non lyphocytic leukaemia (ANLL): 15% of cases; i.e. a 15000 fold increased risk of MDS and ANLL has been evaluated in FA, and it has been assumed that 'it is reasonable to regard the Fanconi anemia genotype as "preleukemia"'; mean age at diagnosis: 13-15 yrs hepatocarcinoma (androgen-therapy induced) in 10%; mean age at diagnosis: 16 yrs

32. Adam Day Learn about a boy who passed away after a fight with fanconi anemia. Find out how to make a donation to the fanconi anemia Research Fund. http://www.adam.interactiveinc.com/

Posted by Darla on February 28, 1997 at 03:02:11: Soaring with angels Greetings All: We, again would like to thank everyone for their sincere and heartfelt support. We literally could not have come as far as we did without all of you. We regretfully inform you all that Adam passed away at 9:11 PM, Minnesota time, on February 27, 1997. He was peaceful and pain-free when he passed. His family was with him, as was most of the staff from 4A, who have care for him in the entire duration of our stay here. We will happily inform everyone, though that Adam is now soaring with the angels, watching down protectively on all of us. We're sure he is having go-cart races with Mark Muellen and showing his knife collection to Joey Adamson and fishing with John Dumouchel. We will miss him but we know he is in a better place. May God bless all of you and shower you with goodness, health and many miracles. Thank you again. The Day Family Adam's Uncle Bob went to Minnesota during 1/30-2/3 and took some photos. Adam was in great spirits despite the constant interruptions by a wide variety of physicians and assistants. Go to: http://www.geocities.com/Heartland/Hills/2219/

33. Short Description Of Cell Lines. Pathology Fanconi Anemia Version 4.200205, Short description of cell lines. Pathology Fanconianemia OMIM Home. By selecting the cell line name, you will http://www.biotech.ist.unige.it/cldb/pat32.html

34. MEDLINEplus: Anemia Blood Donor Anemia (Mayo Foundation for Medical Education and Research); WhatIs fanconi anemia and How Is It Diagnosed? (fanconi anemia Research Fund). http://www.nlm.nih.gov/medlineplus/anemia.html

Skip navigation Other health topics: A B C D ... List of All Topics Anemia Contents of this page: News General/Overviews Diagnosis/Symptoms Research ... Women Search MEDLINE for recent research articles on Anemia: General Aplastic Hemolytic You may also be interested in these MEDLINEplus related pages: Folic Acid Sickle Cell Anemia Blood/Lymphatic System Latest News FDA Uncovers Contaminated Lots of Fake Anemia Drug (03/11/2003, Reuters Health) FDA Statement on Counterfeit Procrit (03/11/2003, Food and Drug Administration) General/Overviews Anemia: When Low Blood Iron is the Cause (American Academy of Family Physicians) Also available in: Spanish What Is Anemia? (Mayo Foundation for Medical Education and Research) Clinical Trials ClinicalTrials.gov: Anemia (National Institutes of Health) ClinicalTrials.gov: Anemia, Aplastic (National Institutes of Health) ClinicalTrials.gov: Thalassemia (National Institutes of Health) Diagnosis/Symptoms Understanding Your Complete Blood Count (National Institutes of Health, Clinical Center) Also available in: Spanish Research Pregnancy Outcomes in Women with Aplastic Anemia Treated with Immunosuppression (American College of Physicians) Reversibility of Liver Scarring in Patients Who Are Cured of Thalassemia (American College of Physicians) Specific Conditions/Aspects Anemia (Normocytic Anemia) (American Academy of Family Physicians) Anemia in Kidney Disease and Dialysis (National Institute of Diabetes and Digestive and Kidney Diseases) Aplastic Anemia (Mayo Foundation for Medical Education and Research)

35. Center For Jewish Genetic Disorders | Fanconi Anemia Information about fanconi anemia and other genetic disorders which are unusuallycommon in Jews of eastern European descent, including symptoms, inheritance http://www.jewishgenetics.org/fanane.htm

Fanconi anemia is a disorder characterized by a reduced production of all types of blood cells in the body. The most serious problem associated with this disorder is an increased risk for cancer. The underlying problem in this condition affects how the genetic information is copied in the cells of the body. The disorder can be seen in individuals from any ethnic background, but one specific gene alteration has been noted in individuals of Jewish ancestry. No effective treatment exists at this time. Disease frequency: Unknown Carrier frequency: Approximately 1 in 89 for a specific gene alteration noted in those of Jewish ancestry. Diagnosis: By a specialized type of chromosome testing or specific testing of one of the genes involved in Fanconi anemia. Inheritance: Autosomal Recessive Carrier testing: Available by testing for a specific gene alteration. Testing detects 95% of carriers for this specific type of Fanconi anemia. Prenatal diagnosis: Available through genetic testing in couples with a previous affected child or couples identified as being carriers.

36. HealthlinkUSA Fanconi Anemia Links medical and health related topics. FindWhat. Click here for page 1of fanconi anemia information from the HealthlinkUSA directory. http://www.healthlinkusa.com/110ent.htm

37. Fanconi Anemia; Treatment, Prevention, Cure fanconi anemiaSearch information from many of the best fanconi anemia health sites. Clickhere to go to the next page of fanconi anemia links 1 2 3 4 5 Next http://www.healthlinkusa.com/content/110.html

Latest Health News Find Drug Information Health Calculators All Words Any Words A B C D ... Z Sunday, March 30, 2003 Alternative therapy struggles to bridge East-West divide Click here to read more Doctors are not following guidelines recommending flu and pneumonia vaccinations for hospitalized adults, leaving millions of elderly patients vulnerable to potentially deadly ailment Click here to read more A helping hand for uninsured; Agencies find ways to provide health care for area children Click here to read more The government has approved the first generic version of the acne drug, Accutane Click here to read more Gates to give India $100m for AIDS; Microsoft CEO begins controversy-laced trip to fight virus Click here to read more Allergies and Asthma Alternative Medicine Arthritis and Your Health ... Women's Health Sunday March 30, 2003 Spina Bifida: Spina Bifida is a rare birth disorder, affecting approximately 1 in 12-1400 live births. Click here to learn more Craniosynostosis: Sagittal Synostosis...males are affected about three times as often as females. Click here to learn more Spinal Cord Injury: Acts of violence have now overtaken falls as the second most common source of spinal cord injury.

38. Nature Publishing Group p 1259 Cellular function of the fanconi anemia pathway Alan D. D'Andrea Harvard MedicalSchool Boston, Massachusetts, USA email alan_dandrea@dfci.harvard.edu. http://www.nature.com/cgi-taf/DynaPage.taf?file=/nm/journal/v7/n12/full/nm1201-1

39. Nature Publishing Group doi10.1038/nm12011259b December 2001 Volume 7 Number 12 pp 1259 - 1260 Replyto 'Cellular function of the fanconi anemia pathway' Robert C. Cumming 1 http://www.nature.com/cgi-taf/DynaPage.taf?file=/nm/journal/v7/n12/full/nm1201-1

40. Fanconi Anemia fanconi anemia is an inherited disorder characterized by a reduced number ofall types of blood cells in the body, leading to bone marrow failure. http://www.einstein.edu/e3front.dll?durki=7171

A  B  C  D  E  F  G  H  I  J  K  L  M  N  O  P  Q  R  S  T  U  V  W  X  Y  Z

Page 2     21-40 of 105    Back | 1  | 2  | 3  | 4  | 5  | 6  | Next 20