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- W2090093118 abstract "Defects of 3q in bands q21 and q26 have been reported in more than 70 cases of acute nonlymphocytic leukemia (ANLL), myelodysplastic syndrome (MDS), and myeloproliferative disorder (MPD) in blast crisis. In this paper three additional patients are described: patient 1 with refractory anemia with excess of blasts in transformation (RAEB-T) and inv(3)(q21q26), patient 2 with RAEB-T and t(3;3)(q21;q26), and patient 3 with myelofibrosis with myeloid metaplasia (MMM) in blast crisis and inv(3)(q21q26). In addition to 3q rearrangements, monosomy 7 and del(7)(q22q36) were observed in patients 1 and 2, respectively. In the three patients, the most characteristic clinical features were elevated platelet counts, marked hyperplasia with dysplasia of the megakaryocytes, and poor prognosis. Although disturbance of thrombopoiesis was not systematically observed in all patients with t(3;3)(q21;q26), inv(3)(q21q26), and ins or dup(3)(q21----q26), study of the 77 cases reported and of the three cases presented here brings further evidence to the existence of a cytogenetic syndrome involving bands q21 and q26 simultaneously, which represents a subtype of ANLL, MDS, and MPD, characterized by normal or elevated platelet counts, hyperplasia with dysplasia of megakaryocytes, multilineage involvement, young median age of patients with MDS, preferential involvement of women in t(3;3), high incidence of chromosome 7 defects in MDS and ANLL, short duration of the MDS phase, no response to chemotherapy, short survival, and por prognosis." @default.
- W2090093118 created "2016-06-24" @default.
- W2090093118 creator A5032971183 @default.
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- W2090093118 creator A5043878680 @default.
- W2090093118 creator A5044758691 @default.
- W2090093118 creator A5055504077 @default.
- W2090093118 date "1992-04-01" @default.
- W2090093118 modified "2023-09-26" @default.
- W2090093118 title "Three new cases of chromosome 3 rearrangement in bands q21 and q26 with abnormal thrombopoiesis bring further evidence to the existence of a 3q21q26 syndrome" @default.
- W2090093118 cites W147310725 @default.
- W2090093118 cites W1483807376 @default.
- W2090093118 cites W1484310192 @default.
- W2090093118 cites W1492963656 @default.
- W2090093118 cites W1540955949 @default.
- W2090093118 cites W1550033196 @default.
- W2090093118 cites W1560043555 @default.
- W2090093118 cites W1679570532 @default.
- W2090093118 cites W1904815093 @default.
- W2090093118 cites W1964509813 @default.
- W2090093118 cites W1969141341 @default.
- W2090093118 cites W1975555731 @default.
- W2090093118 cites W1977616802 @default.
- W2090093118 cites W1983171249 @default.
- W2090093118 cites W1984010327 @default.
- W2090093118 cites W1986996454 @default.
- W2090093118 cites W1993071663 @default.
- W2090093118 cites W1995347606 @default.
- W2090093118 cites W2001385364 @default.
- W2090093118 cites W2002783109 @default.
- W2090093118 cites W2002966604 @default.
- W2090093118 cites W2004169591 @default.
- W2090093118 cites W2006178295 @default.
- W2090093118 cites W2008379494 @default.
- W2090093118 cites W2013309598 @default.
- W2090093118 cites W2013895550 @default.
- W2090093118 cites W2018248988 @default.
- W2090093118 cites W2018809606 @default.
- W2090093118 cites W2019685656 @default.
- W2090093118 cites W2021277771 @default.
- W2090093118 cites W2024305087 @default.
- W2090093118 cites W2025484402 @default.
- W2090093118 cites W2026153092 @default.
- W2090093118 cites W2026461778 @default.
- W2090093118 cites W2032020623 @default.
- W2090093118 cites W2032361124 @default.
- W2090093118 cites W2046696992 @default.
- W2090093118 cites W2046845363 @default.
- W2090093118 cites W2048187686 @default.
- W2090093118 cites W2048744141 @default.
- W2090093118 cites W2053487253 @default.
- W2090093118 cites W2057291706 @default.
- W2090093118 cites W2057362691 @default.
- W2090093118 cites W2058151507 @default.
- W2090093118 cites W2061133964 @default.
- W2090093118 cites W2065086233 @default.
- W2090093118 cites W2067150248 @default.
- W2090093118 cites W2069932116 @default.
- W2090093118 cites W2070348803 @default.
- W2090093118 cites W2071654561 @default.
- W2090093118 cites W2073001484 @default.
- W2090093118 cites W2076615810 @default.
- W2090093118 cites W2077687523 @default.
- W2090093118 cites W2077962097 @default.
- W2090093118 cites W2078652096 @default.
- W2090093118 cites W2079574988 @default.
- W2090093118 cites W2082596119 @default.
- W2090093118 cites W2086049053 @default.
- W2090093118 cites W2086884711 @default.
- W2090093118 cites W2087110785 @default.
- W2090093118 cites W2087130577 @default.
- W2090093118 cites W2091214957 @default.
- W2090093118 cites W2092149157 @default.
- W2090093118 cites W2102054322 @default.
- W2090093118 cites W2106493687 @default.
- W2090093118 cites W2109374739 @default.
- W2090093118 cites W2135230436 @default.
- W2090093118 cites W2150113701 @default.
- W2090093118 cites W22328419 @default.
- W2090093118 cites W2275994791 @default.
- W2090093118 cites W2316282026 @default.
- W2090093118 cites W2333326790 @default.
- W2090093118 cites W2333476784 @default.
- W2090093118 cites W2364667991 @default.
- W2090093118 cites W2384198704 @default.
- W2090093118 cites W2404827353 @default.
- W2090093118 cites W2405099813 @default.
- W2090093118 cites W2412689496 @default.
- W2090093118 cites W2417381454 @default.
- W2090093118 cites W2417547808 @default.
- W2090093118 cites W2426745600 @default.
- W2090093118 cites W2470741139 @default.
- W2090093118 cites W4236296592 @default.
- W2090093118 cites W4240354264 @default.
- W2090093118 cites W4248300473 @default.
- W2090093118 cites W4253916874 @default.
- W2090093118 doi "https://doi.org/10.1016/0165-4608(92)90208-p" @default.
- W2090093118 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/1581880" @default.