17qトリソミー
WordNet
- chrosomal abnormality in which there is one more than the normal number of chromosomes in a cell
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English Journal
- Partial trisomy 17q and partial monosomy 20q in a boy with craniosynostosis.
- Marques F1, Heredia R, de Oliveira C, Cardoso MT, Mazzeu J, Pogue R.
- American journal of medical genetics. Part A.Am J Med Genet A.2015 Feb;167(2):412-6. doi: 10.1002/ajmg.a.36844. Epub 2014 Nov 25.
- Craniosynostosis is defined as a premature fusion of at least one cranial suture, which can be accompanied by other findings. Of syndromic cases, 14-22% have been associated with chromosomal rearrangements. This report describes a Brazilian boy with syndromic craniosynostosis who also presented with
- PMID 25424318
- Transformed aggressive γδ-variant T-cell large granular lymphocytic leukemia with acquired copy neutral loss of heterozygosity at 17q11.2q25.3 and additional aberrations.
- Zhang L1, Ramchandren R, Papenhausen P, Loughran TP, Sokol L.
- European journal of haematology.Eur J Haematol.2014 Sep;93(3):260-4. doi: 10.1111/ejh.12313. Epub 2014 Apr 7.
- T-cell large granular lymphocytic leukemia (T-LGLL) is a rare indolent lymphoproliferative disorder characterized by cytopenias, splenomegaly, and various degrees of T-cell lymphocytosis, due to a clonal expansion of CD8-positive cytotoxic T-cells. Phenotypic variants of T-LGLL include CD4(+) /CD8(-
- PMID 24635703
- Molecular cytogenetic characterization of mammary neuroendocrine carcinoma.
- Xiang DB1, Wei B2, Abraham SC3, Huo L3, Albarracin CT3, Zhang H3, Babiera G4, Caudle AS4, Akay CL4, Rao P5, Zhao YJ5, Lu X6, Wu Y7.
- Human pathology.Hum Pathol.2014 Sep;45(9):1951-6. doi: 10.1016/j.humpath.2014.06.002. Epub 2014 Jun 18.
- Primary mammary neuroendocrine carcinoma (NEC) is an uncommon entity that accounts for 2% to 5% of breast carcinomas. Recent reports have shown that NEC of the breast is an aggressive subtype of mammary carcinoma that is distinct from invasive ductal carcinoma, not otherwise specified, and have sugg
- PMID 25074542
Japanese Journal
- 14/X染色体転座により14q部分トリソミーを呈した1例
- 池住 洋平,渡辺 輝浩,押阪 裕之,北谷 真潮
- 日本小児科学会雑誌 101(6), 1096-1101, 1997-06-01
- NAID 10005653745
Related Links
- Trisomy 17q symptoms, causes, diagnosis, and treatment information for Trisomy 17q (Chromosome 17q, partial duplication) with alternative diagnoses, full-text book chapters, misdiagnosis, research treatments, prevention, and ...
- Chromosome 17q trisomy symptoms, causes, diagnosis, and treatment information for Chromosome 17q trisomy (Chromosome 17q, partial duplication) with alternative diagnoses, full-text book chapters, misdiagnosis, research ...
★リンクテーブル★
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- 英
- trisomy 17q
- 関
- 17番染色体