ECHOGRAPHIC FINDINGS IN FETUS WITH TURNER SYNDROME

Authors

  • Tábata de O. Silva
  • Carlos Eduardo L. de S. Cruz
  • João Pedro C. Correia
  • Paula de O. Silva
  • Jobe Petter

Keywords:

TURNER SYNDROME, FETAL MEDICINE, CHROMOSOMAL DISEASE, NUCHAL TRANSLUCENCY, ULTRASONOGRAPHY

Abstract

Turner Syndrome (TS) is the congenital hypoplastic ovarian syndrome that occurs in the absence or partiality of the X chromosome and by instability of the Y chromosome, which causes loss during meiosis. Diagnosis by ultrasound examination in the 1st and 2nd trimester is essential to identify phenotypic changes and associated complications with the pathology, such as those seen in the current case.

Published

2021-09-01

How to Cite

1.
Silva T de O, Cruz CEL de S, Correia JPC, Silva P de O, Petter J. ECHOGRAPHIC FINDINGS IN FETUS WITH TURNER SYNDROME . RBUS [Internet]. 2021 Sep. 1 [cited 2025 Jan. 18];29(31). Available from: https://revistarbus.sbus.org.br/rbus/article/view/259