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A Case of Haemobartonellosis in a Cat in Istanbul OAK
Tüzer, Erkut; Göksu, Kamil; Bilal, Tarik; Yesildere, Tahsin.
Palavras-chave: Haemobartonellosis; Cat; Case report; In Turkey.
Ano: 1993 URL: http://ir.obihiro.ac.jp/dspace/handle/10322/188
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A Clinical Case of Severe Anemia in a Sheep Coinfected with Mycoplasma ovis and 'Candidatus Mycoplasma haemovis' in Hokkaido, Japan OAK
TAGAWA, Michihito; TAKEUCHI, Toshihiko; FUJISAWA, Tetsuro; KONNO, Yasuhiro; YAMAMOTO, Shinji; MATSUMOTO, Kotaro; YOKOYAMA, Naoaki; INOKUMA, Hisashi; 松本, 高太郎; 横山, 直明; 猪熊, 壽.
A 2-year-old East Friesian sheep imported from Australia exhibited severe anemia after contagious pustular dermatitis in Hokkaido, Japan. Hemoplasma infection was confirmed in blood smears. Both Mycoplasma ovis and ‘Candidatus Mycoplasma haemovis’ were detected by PCR and sequence analyses. In the epidemiological analysis, dual pathogens were detected in 6 of 12 (50.0%) sheep imported from Australia with the infected ewe at the same time, 1 of 5 (20.0%) sheep introduced from a domestic farm in Hokkaido, and in 1 of 16 (6.3%) sheep from an epidemiologically unrelated ranch. It is the first clinical case of sheep to confirm coinfection of these pathogens in Japan.
Palavras-chave: 'Candidatus Mycoplasma haemovis'; Case report; Japan; Mycoplasma ovis; Sheep.
Ano: 2012 URL: http://ir.obihiro.ac.jp/dspace/handle/10322/3582
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Clinical and cytogenetic characterization of a patient with tetrasomy 18p JBAG
Vazquez Cantú,D.L; Gutiérrez García,V.M; Cruz-Camino,H; Lara Díaz,V.J; Garza García,K; Garduño Zarazúa,L.M; Meléndez Hernández,R; Paz Martínez,A; Mayén Molina,D.G; Cantú-Reyna,C.
The 18p tetrasomy is a structural chromosomal abnormality with the presence of an extra isochromosome 18p, caused by a nondisjunction failure during maternal meiosis II. This additional i(18p) occurs in 1 of 180,000 live-born children worldwide, affecting males and females equally. It is characterized by craniofacial dysmorphisms; ears, nose and throat (ENT) abnormalities; musculoskeletal alterations; and global development delay. We aim to present the clinical and cytogenetic findings of a 3-year-10-month-old Latin American male with i(18p), to support the gene dosage effects, comparing his features with the ones reported in literature. This patient was product of the second pregnancy of a 39-year-old woman and the first son of a 49-year-old man. His main...
Tipo: Info:eu-repo/semantics/article Palavras-chave: Tetrasomy 18p; Chromosome 18; Isochromosome; Cytogenetic analysis; Case report.
Ano: 2018 URL: http://www.scielo.org.ar/scielo.php?script=sci_arttext&pid=S1852-62332018000100002
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