Fletcher Allen, a Vermont university hospital and medical center, serves all of
Vermont and the northern New York region. Located in Burlington, Fletcher Allen is a regional, academic healthcare center and teaching hospital in alliance with the University of Vermont.
National Organization for Rare Disorders, Inc.
It is possible that the main title of the report Fanconi Anemia is not the name you expected. Please check the synonyms listing to find the alternate name(s) and disorder subdivision(s) covered by this report.
- Fanconi's Anemia, Type I (FA1)
- Fanconi Pancytopenia
- Fanconi's Anemia, Estren-Dameshek Variant
- Aplastic Anemia with Congenital Anomalies
- Congenital Pancytopenia
- Constitutional Aplastic Anemia
- Fanconi Panmyelopathy
- Fanconi's Anemia, Complementation Group A (FANCA); FAA
- Fanconi's Anemia, Complementation Group B (FANCB); FACB
- Fanconi's Anemia, Complementation Group C (FANCC); FAC
- Fanconi's Anemia, Complementation Group D (FANCD); FACD
- Fanconi's Anemia, Complementation Group E (FANCE); FACE
- Fanconi's Anemia, Complementation Group F (FANF); FACF
- Fanconi's Anemia, Complementation Group G (FANG); FACG
- Fanconi's Anemia, Complementation Group H (FANH); FACH
Fanconi anemia (FA) is a rare genetic disorder, in the category of inherited bone marrow failure syndromes. Half the patients are diagnosed prior to age 10, while about 10 % are diagnosed as adults. Early diagnoses are facilitated in patients with birth defects, such as small size, abnormal thumbs and/or radial bones, skin pigmentation, small heads, small eyes, abnormal kidney structures, and cardiac and skeletal anomalies. The disorder is often associated with a progressive deficiency of all bone marrow production of blood cells, red blood cells, white blood cells, and platelets. Affected individuals have an increased risk of developing a cancer of blood-forming cells in the bone marrow called acute myeloid leukemia (AML), or tumors of the head, neck, skin, gastrointestinal system, or genital tract. FA occurs equally in males and females, and is found in all ethnic groups. It is usually inherited as an autosomal recessive genetic disorder, but X-linked inheritance has also been reported.
There are several subtypes of FA that result from the inheritance of two gene mutations in each of 15 different genes. Most of the subtypes share the characteristic symptoms and findings.
FA is not related to the same as Fanconi syndrome, a rare kidney functional disorder.
March of Dimes Birth Defects Foundation
1275 Mamaroneck Avenue
White Plains, NY 10605
Fanconi Anemia Research Fund, Inc.
1801 Willamette St
Eugene, OR 97401
International Fanconi Anemia Registry
c/o Arleen Auerbach Ph.D.
1230 York Avenue
New York, NY 10021
NIH/National Heart, Lung and Blood Institute
P.O. Box 30105
Bethesda, MD 20892-0105
Canadian Fanconi Anemia Research Fund
PO Box 38157
Ontario, M5N 3A9
NIH/National Heart, Lung and Blood Institute ~ Hematology Branch
10 Center Dr, Building 10-CRC
Bethesda, MD 20892-1202
Genetic and Rare Diseases (GARD) Information Center
PO Box 8126
Gaithersburg, MD 20898-8126
PO Box 241956
Los Angeles, CA 90024
Let Them Hear Foundation
1900 University Avenue, Suite 101
East Palo Alto, CA 94303
PO Box 905
Hants, PO1 9JG
For a Complete Report
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The information provided in this report is not intended for diagnostic purposes. It is provided for informational purposes only. NORD recommends that affected individuals seek the advice or counsel of their own personal physicians.
It is possible that the title of this topic is not the name you selected. Please check the Synonyms listing to find the alternate name(s) and Disorder Subdivision(s) covered by this report
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Last Updated: 1/14/2013
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