Project description:Two case reports with multifocal infections due to Campylobacter fetus
| PRJEB35508 | ENA
Project description:Different outcomes following parathyroidectomy in patients with uremic tumoral calcinosis: two case reports
| PRJNA910968 | ENA
Project description:Whole-genome sequencing confirmed coinfection of Mycobacterium ulcerans-infected lesions with Rhodococcus erythropolis: Two case reports.
Project description:Isolated deletions of the long arm of chromosome 5 (del(5q)) are observed in 10% of myelodysplastic syndromes (MDS) and are associated with a more favorable prognosis, although the clinical course varies considerably. If one or more additional chromosomal aberration/s are present this correlates with a significant shorter overall survival. To assess the frequency of hidden abnormalities in cases with an isolated cytogenetic del(5q), we have performed a genome wide high resolution 44K 60mer oligonucleotide array CGH study using DNA from bone marrow cells of 12 MDS and one AML patient. Additional chromosomal aberrations were identified in three of 13 cases (23%): in one case, a single additional hidden 5.6 Mb deletion of 13q14 and in two cases, multiple larger aberrations involving many chromosomes. Fluorescence in situ hybridization (FISH) demonstrated that aberrations present in only 10% of the bone marrow cells were detectable by aCGH. Furthermore with oligonucleotide aCGH the deletion end points in 5q were mapped precisely, revealing a cluster of proximal break points in band q14.3 (n=8) and a distal cluster between bands q33.2 to q34 (n=11). This study shows the high resolution of oligonucleotide CGH arrays for precisely mapping genomic alterations and for refinement of deletion end points. In addition the high sensitivity of this method enables the study of whole bone marrow cells from MDS patients, a disease with a low blast count. Future studies of more patients with isolated del(5q) for hidden abnormalities will be necessary to evaluate the impact of these on the variable prognosis in these patients and to further define new genetic subgroups. Keywords: Myelodysplastic syndromes, MDS, array CGH, del(5q), hidden aberrations
2007-09-11 | GSE8804 | GEO
Project description:COINCIDENCE OF PRIMARY ADRENOCORTICAL CARCINOMA AND MELANOMA: THREE CASE REPORTS
Project description:Faecal microbiota transplantation for immune checkpoint inhibitor-induced colitis is safe and contributes to recovery: two case reports
| PRJEB51242 | ENA
Project description:Co-occurrence of Erdheim-Chester Disease and Acute Myeloid Leukemia
| PRJNA1073715 | ENA
Project description:Putative pathogenic genes of Leptospira interrogans and Leptospira weilii isolated from patients with acute febrile illness: Two case reports
| PRJNA823851 | ENA
Project description:Unveiling the hidden diversity and functional role of Chloroflexota in full-scale wastewater treatment plants through genome-centric analyses