000 02445cam a2200349 a 4500
003 EG-GiCUC
005 20250223032544.0
008 200822s2020 ua dh f m 000 0 eng d
040 _aEG-GiCUC
_beng
_cEG-GiCUC
041 0 _aeng
049 _aDeposite
097 _aPh.D
099 _aCai01.19.03.Ph.D.2020.La.N
100 0 _aLamiaa Nabih Helal Elfadali
245 1 0 _aNucleophosmin mutations in De novo adult acute myeloid leukemia and its prognostic impact /
_cLamiaa Nabih Helal Elfadali ; Supervised Khaled Mostafa Aboulenein , Naglaa Mostafa Hassan Ahmed , Raafat Mohammad Abdelfattah
246 1 5 _aدراسة تكرار طفرة جين النيوكليوفوزمين فى حالات سرطان الدم الميلودى الحاد الجديدة لدى البالغين
260 _aCairo :
_bLamiaa Nabih Helal Elfadali ,
_c2020
300 _a143 P. :
_bcharts , facsimiles ;
_c25cm
502 _aThesis (Ph.D.) - Cairo University - National Cancer Institute - Department of Clinical Pathology
520 _aAim:To evaluate the frequency of NPM mutation A in denovo adult AML and to evaluate its relation with clinical and laboratory parameters and with response to treatment. Patients and Methods: 89 patients were included in our study, taking BM samples, RNA extraction and quantitative RT-PCR were done to detect the frequency of NPM1 mutation A. Results:We found NPM1 mutation in 33/89 (37.1) AML patients of which NPM mutation A was found in 6/33 (18.1%) NPM mutated AML patients and was 6/89 (6.7%) of AML patients. 24/33 (72.7%) NPM mutated patients were died before day 28 of treatment. 9/33 (27.3%) NPM mutant patients achieved CR. 5/6 (83.3%) NPM mutation A patients died before D28 of treatment and 1/6 (6.7%) NPM mutation A patient achieve CR with no statistically significance. Conclusions:We found that frequency of NPM gene mutation was 37% of AML patients and NPM gene mutation A was 18% of NPM1 mutation and 6.7 of AML patients
530 _aIssued also as CD
653 4 _aActivities of daily living (ADL)
653 4 _aAcute myeloid leukemia
653 4 _aNucleophosmin gene mutation
700 0 _aKhaled Mostafa Aboulenein ,
_eSupervisor
700 0 _aNaglaa Mostafa Hassan Ahmed ,
_eSupervisor
700 0 _aRaafat Mohammad Abdelfattah ,
_eSupervisor
856 _uhttp://172.23.153.220/th.pdf
905 _aNazla
_eRevisor
905 _aShimaa
_eCataloger
942 _2ddc
_cTH
999 _c77305
_d77305