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  • Journal of Experimental and Clinical Medicine
  • Volume:23 Issue:1
  • X İzokromozomuna Sahip Turner Sendromlu Bir Olgu Sunumu

X İzokromozomuna Sahip Turner Sendromlu Bir Olgu Sunumu

Authors : A GÜVEN, Ş KOÇAK, M AYDIN, G ÖKTEN, G OĞUR
Pages : 29-32
Doi:10.5835/jecm.v23i1.55
View : 33 | Download : 13
Publication Date : 2009-12-30
Article Type : Other Papers
Abstract :A Case Presentation of Turner`s Syndrome with X Isochromosome Classic Turner`s Syndrome which has severe findings is the most common cytogenetic type of Turner`s Syndrome. iinsert ignore into journalissuearticles values(Xq); isochromosome is also a common cytogenetic abnormality and cases have generally milder clinics than classic Turner`s Syndrome. In this report, we present a case of Turner`s Syndrome with a characteristic isochromosome iinsert ignore into journalissuearticles values(Xq); structure which exhibits a milder clinical finding due to the lack of signs such as low posterior hairline, prominent webbed neck, shield chest, kidney and congenital heart abnormalities. Klasik Turner Sendromu Turner Sendromunun en sık görülen sitogenetik tipi olup daha ağır bulgularla seyreder. İzokromozom iinsert ignore into journalissuearticles values(Xq); yapısı ise daha az sıklıkla gözlenen sitogenetik bir anomali olup olgular genelde klasik Turner sendromu`na göre daha hafif bir kliniğe sahiptir. Bu yazıda, klinik olarak düşük saç çizgisi, belirgin yele boyun, kalkan göğüs, böbrek ve konjenital kalp anomalisi bulguları olmayan daha hafif kliniğe sahip izokromozom iinsert ignore into journalissuearticles values(Xq); yapısındaki Turner sendrom`lu bir olgu sunulmaktadır.
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