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Extra X Chromosome in Mosaic Klinefelter Syndrome Is Associated with a Hematologic Malignancy

김선희|정철원|장미애
대한진단검사의학회 (Korean Society For Laboratory Medicine)|2013.07|Annals of Laboratory Medicine|제33권 제4호|pp. 297-299

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참고문헌 (14)

  1. Wikström AM, "Klinefelter syndrome", Best Pract Res Clin Endocrinol Metab, 25, pp.239~250 (2011)
  2. Yamamoto K, "An extra X chromosome as a sole abnormality in relapse of an adult acute lymphoblastic leukemia", Cancer Genet Cytogenet, 155, pp.154~155 (2004)
  3. Tsutsumi Y, "Acute biphenotypic leukemia and an acquired X chromosome", Cancer Genet Cytogenet, 157, pp.94~95 (2005)
  4. Wan TS, "Fatal diffuse alveolar damage complicating acute myeloid leukemia with abnormal eosinophils and trisomy X", Ann Hematol, 81, pp.167~169 (2002)
  5. Yamamoto K, "Acquired gain of an X chromosome as the sole abnormality in the blast crisis of chronic neutrophilic leukemia", Cancer Genet Cytogenet, 134, pp.84~87 (2002)
  6. Hur M, "Cleft palate in a rare case of Variant Klinefelter syndrome with 48,XXXY", 46,XY mosaicism, 2009, pp.46, 555~557
  7. Lanfranco F, "Klinefelter’s syndrome", Lancet, 364, pp.273~283 (2004)
  8. Kruse R, "Genetic counseling in a patient with XXY", XXXY, Fertil Steril, pp.1998, 69[DOI]
  9. Abramsky L, "47,XXY (Klinefelter syndrome) and 47,XYY: estimated rates of and indication for postnatal diagnosis with implications for prenatal counselling", Prenat Diagn, 17, pp.363~368 (1997)
  10. Kamischke A, "Clinical and diagnostic features of patients with suspected Klinefelter syndrome", J Androl, 24, pp.41~48 (2003)
  11. Zeidan A, "Acquired biclonal chromosome X aberrations without autosomal chromosomal anomalies in acute myeloid leukemia", Cancer Genet Cytogenet, 181, pp.125~130 (2008)
  12. Yhim HY, "JAK2 V617F-positive essential thrombocythemia in a patient with Klinefelter syndrome: a case report", CANCER GENETICS AND CYTOGENETICS, 198, pp.162~165 (2010), ELSEVIER SCIENCE INC
  13. Kumar S, "Agnogenic myeloid metaplasia associated with Klinefelter syndrome: a case report", Ann Hematol, 81, pp.215~218 (2002)
  14. Okada H, "Fluorescence in situ hybridization analysis of sex-chromosome mosaicism in azoospermic men", J Androl, 22, pp.970~972 (2001)

관련 논문AI추천

Persistent suboptimal molecular response in a patient with chronic myelogenous leukemia and Klinefelter syndromeKranthi Singam, Natalia Calderon, Rajshekhar Chakraborty, Shiva Kumar Reddy Mukkamalla대한내과학회 · The Korean Journal of Internal Medicine2014 · 제29권 제6호Immature Teratoma and Subsequent Acute Promyelocytic Leukemia in a Pediatric Patient With XYY Syndrome국훈, 강민구, 김수현, 박주현, 백희조, 서보영, 신명근, 최현우대한진단검사의학회 · Annals of Laboratory Medicine2015 · 제35권 제5호Klinefelter Syndrome Identified by Next-Generation Sequencing as a Risk Factor for Venous Thromboembolism: A Single-Institution StudyChang Sung-A, Kim Hee-Jin, Kim Hyun-Young, Lee Jae Joon, Park Chang-Hun, Park Min-Seung, Park Taek Kyu대한진단검사의학회 · Annals of Laboratory Medicine2026 · 제46권 제1호Diagnosis of Variant Klinefelter Syndrome in a 21-Year-Old Male Who Presented with Sparse Facial HairA. Tülin Güleç, Feride Iffet Sahin, Seda Purnak, Simin Ada, Tugce Bulakbasi Balci대한피부과학회 · Annals of Dermatology2012 · 제24권 제3호A Case of Pentasomy 21 With Two Isochromosome 21s in Acute Megakaryoblastic Leukemia Associated With Down Syndrome구선회, 구영현, 권계철, 김지명, 박영찬, 임진숙대한진단검사의학회 · Annals of Laboratory Medicine2015 · 제35권 제3호XYY syndrome: a 13-year-old boy with tall stature권아름, 김기은, 김덕희, 김호성, 정모경, 조원하, 채현욱대한소아내분비학회 · Annals of Pediatric Endocrinology & Metabolism2015 · 제20권 제3호

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