- Fanconi's Anemia
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Kim SK, Kim HK, Kim KT
- KMID: 2208672
- J Korean Pediatr Soc.
- 1981 Aug;24(8):782-785.
We report 1 case of Fanconi's anemia which has severe pancytopenia, PDA, hypoplatic right thumb and cryptorchism with a brief review of related literature and references. -
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- Treatment of Tongue Cancer in Patient with Fanconi's Anemia
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Lee SH, Park HS, Chang JW, Koo BS
- KMID: 2392972
- Korean J Otorhinolaryngol-Head Neck Surg.
- 2017 Sep;60(9):467-470.
- doi: 10.3342/kjorl-hns.2016.16565
Fanconi's anemia is a rare autosomal recessive genetic disorder characterized by congenital abnormalities and anaplastic anemia. Patients with this disorder has predisposition for leukemia, specifically acute myeloid leukemia. Risk for... -
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- Fanconi Anemia
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Lee SI, Koh YY, Suh JG, Ahn HS, Hong CY
- KMID: 2103983
- J Korean Pediatr Soc.
- 1981 Feb;24(2):153-163.
No abstract available. -
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- A Case of Fanconi's Anemia
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Cha DH, Choi JS, Kim KH, Lee HK, Hahn SS
- KMID: 1699096
- J Korean Pediatr Soc.
- 1983 Aug;26(8):808-811.
No abstract available. -
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- Fanconi's Anemia
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Yoo JH, Kim EM, Lee SJ, Kim WB, Lee DW, Choi KY, Kang DY
- KMID: 1699034
- J Korean Pediatr Soc.
- 1983 Nov;26(11):1139-1144.
No abstract available. -
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- Unrelated Cord Blood Transplantation Using Non-TBI Conditioning Regimen in a Child with Fanconi Anemia
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Park SS, Park JA, Lim YT
- KMID: 2279858
- Clin Pediatr Hematol Oncol.
- 2007 Apr;14(1):68-72.
Fanconi anemia is an autosomal recessive disorder characterized by progressive bone marrow failure, growth retardation, abnormal skin pigmentation, developmental anomalies and marked predisposition to myelodysplastic syndrome or acute myeloid leukemia.... -
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- Triplication of 1q in a Patient with Myelodysplastic Syndrome
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Cho HS, Kim MK, Hyun MS
- KMID: 2252329
- Korean J Hematol.
- 2006 Mar;41(1):56-60.
- doi: 10.5045/kjh.2006.41.1.56
Triplication of 1q is a very rare chromosomal abnormality in hematologic malignancies, and it has been related to Fanconi anemia. The clinical significance of this abnormality is unknown. We report... -
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- Inactivation of the NHEJ Activity of DNA-PKcs Prevents Fanconi Anemia Pre-Leukemic HSC Expansion
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Chatla S, Wilson AF, Pang Q
- KMID: 2465886
- Int J Stem Cells.
- 2019 Nov;12(3):457-462.
- doi: 10.15283/ijsc19074
Fanconi anemia (FA) is a genetic disorder characterized by bone marrow failure and high risk of cancer particularly leukemia. Here we show that inactivation of the non-homologous end-joining (NHEJ) activity... -
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- Overexpression of the Fanconi Anemia A Gene in Hela and MCF10A Cells
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Park WH
- KMID: 2252321
- Korean J Hematol.
- 2006 Mar;41(1):1-7.
- doi: 10.5045/kjh.2006.41.1.1
BACKGROUND: Fanconi Anemia (FA) is an autosomal recessive inherited disease, which is characterized by developmental abnormalities, progressive bone marrow failure and a predisposition to cancer. The phenotypes of FA cells... -
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- Growth Hormone Treatment for Fanconi Anemia with Growth Hormone Deficiency
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Kim MK, Kang MJ, Chung HR, Shin CH, Yang SW
- KMID: 2192852
- J Korean Soc Pediatr Endocrinol.
- 2010 Dec;15(3):198-202.
Short stature is common in case of Fanconi anemia (FA) and may result from inherent abnormalities of FA or endocrinopathies, such as a growth hormone deficiency and hypothyroidism. Growth hormone... -
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- A Case of Fanconi Anemia Diagnosed by a Chromosome Breakage Test with Skin Fibroblasts
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Lee JJ, Yun KB, Kim SY, Lee MJ, Jung HJ, Park JE, Kim HJ
- KMID: 1485160
- Korean J Hematol.
- 2008 Mar;43(1):62-67.
- doi: 10.5045/kjh.2008.43.1.62
Fanconi anemia is an autosomal recessive disease that's characterized by congenital anomalies, defective hematopoiesis and a high risk of developing acute myeloid leukemia and certain solid tumors. The clinical phenotype... -
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- Gefitinib Trial in a Fanconi's Anemia Patient with Multiple Squamous Cell Carcinomas and Hepatocellular Carcinoma
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Jung HS, Byun GW, Lee KE, Mun YC, Nam SH, Kwon JM, Lee SN, Im SA, Seong CM, Lee SN
- KMID: 2166112
- Cancer Res Treat.
- 2005 Dec;37(6):370-373.
FA (Fanconi's Anemia) is an autosomal recessive disorder that is characterized by pancytopenia with bone marrow hypoplasia, diverse congenital abnormalities and an increased predisposition towards malignancy. The mainstay of the... -
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- Chromosome Breakage Test for the Diagnosis of Fanconi's Anemia
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Ryang DW, Cho D, Hong WP, Kook H, Hwang TJ
- KMID: 1863298
- Korean J Clin Pathol.
- 1998 Mar;18(1):101-106.
BACKGROUND: Fanconi's anemia (FA) is an autosomal recessive disease characterized by aplastic anemia, pre-malignancy, congenital malformations and chromosome breakage syndromes. As up to 30% of patients have no detectable congenital... -
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- Squamous Cell Carcinoma of Oral Cavity and Metachronously Developed Hepatocellular Carcinoma Arising from Fanconi's Anemia
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Min JS, Park JH, Shin DG, Kim IS
- KMID: 1940514
- J Korean Surg Soc.
- 2006 Feb;70(2):148-152.
Fanconi's anemia (FA) is a rare familiar form of aplastic anemia (AA) that is associated with increased chromosomal instability and defective DNA repair, and it characterized by progressive pancytopenia, skeletal... -
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- A Case Report of Fanconi Anemia Diagnosed by Genetic Testing Followed by Prenatal Diagnosis
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Lee HJ, Park S, Kang HJ, Jun JK, Lee JA, Lee DS, Park SS, Seong MW
- KMID: 1387356
- Ann Lab Med.
- 2012 Sep;32(5):380-384.
- doi: 10.3343/alm.2012.32.5.380
Fanconi anemia (FA) is a rare genetic disorder affecting multiple body systems. Genetic testing, including prenatal testing, is a prerequisite for the diagnosis of many clinical conditions. However, genetic testing... -
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- A Clinical Study of Fanconi's Anemia
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Cho SH, Kook H, Kim GM, Yoon WS, Cho TH, Hwang TJ
- KMID: 2072456
- Korean J Pediatr Hematol Oncol.
- 1997 Apr;4(1):70-77.
BACKGROUND: Fanconi's anemia(FA) is an autosomal recessive disease characterized by aplastic anemia and congenital malformations. As up to 30% of patients have no physical stigmata, the modern diagnosis of FA... -
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- Silencing of Fanconi Anemia Complementation Group F Exhibits Potent Chemosensitization of Mitomycin C Activity in Breast Cancer Cells
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Yu J, Zhao L, Li Y, Li N, He M, Bai X, Yu Z, Zheng Z, Mi X, Wang E, Wei M
- KMID: 2286380
- J Breast Cancer.
- 2013 Sep;16(3):291-299.
- doi: 10.4048/jbc.2013.16.3.291
PURPOSE: Fanconi anemia complementation group F (FANCF) is a key factor to maintaining the function of Fanconi anaemia/BRCA (FA/BRCA) pathway, a DNA-damage response pathway. However, the functional role of FANCF... -
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- Infant with Fanconi Anemia Presenting with Myelodysplastic Syndrome
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Cho TH, Kook H, Ryu NE, Kim CJ, Lee JH, Hwang TJ
- KMID: 1535337
- Korean J Pediatr Hematol Oncol.
- 1998 Oct;5(2):322-327.
PURPOSE: Fanconi anemia(FA) is a rare autosomal recessive disorder characterized by progressive bone marrow failure and congenital malformations. Patients with FA have aplastic anemia(> 90%), leukemia(10~15%), myelodysplasia(5%) and liver(5%) and... -
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- Comparison of Combined Immune Suppression, Bone Marrow Transplantation and Androgen Treatment in Childhood Severe Aplastic Anemia
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Hwang MJ, Kook H, Kim CJ, Park HJ, Kim SY, Park A, Hwang TJ
- KMID: 1535331
- Korean J Pediatr Hematol Oncol.
- 1998 Oct;5(2):266-277.
PURPOSE: The purpose of this study is to compare treatment response and survival according to treatment modalities, such as allogeneic bone marrow transplantation (BMT), combined immunosuppression and supportive care, and... -
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- Long-term follow-up of Fanconi anemia: clinical manifestation and treatment outcome
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Yoon BG, Kim HN, Han UJ, Jang HI, Han DK, Baek HJ, Hwang TJ, Kook H
- KMID: 1702651
- Korean J Pediatr.
- 2014 Mar;57(3):125-134.
- doi: 10.3345/kjp.2014.57.3.125
PURPOSE: The aim of this study was to characterize Korean patients with Fanconi anemia (FA), which is a rare but very challenging genetic disease. METHODS: The medical records of 12 FA... -
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