[Revisiting establishments of the etiology of Turner syndrome].

نویسندگان

  • Monica de Paula Jung
  • Maria Helena Cabral de Almeida Cardoso
  • Maria Auxiliadora Monteiro Villar
  • Juan Clinton Llerena
چکیده

Based on an interview with José Carlos Cabral de Almeida, who took part in the investigative process, the article explores the research that culminated in the establishment of the genetic etiology of Turner syndrome. Cabral de Almeida also discusses other work that he sees as landmarks in the birth of cytogenetics and offers his current view of the development of clinicalgenetics and the important role played by cytogenetics, which affords more precise means of diagnosis, prognosis, and control ofgenetic disorders. In its conclusion, the article points to pioneer work that continues to impact medical genetics, especially the study of human chromosomes, still fundamental to the success of linking human genetics and disease processes.

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منابع مشابه

Simultaneous Occurrence of Turner Syndrome and Robertsonian Translocation in a Girl with Short Stature: A Case Report

Short stature is an important clinical feature of Turner syndrome (TS). In this report, a girl with short stature suspected to have Turner syndrome underwent cytogenetic analysis, which confirmd Turner syndrome by observing sex chromosomal monosomy using the karyotype test. In addition to Turner syndrome, Robertsonian (ROB) translocation t(13;14) was detected. As recommended by a genetic counse...

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عنوان ژورنال:
  • Historia, ciencias, saude--Manguinhos

دوره 16 2  شماره 

صفحات  -

تاریخ انتشار 2009