How is Turner Syndrome diagnosed?

A diagnosis of Turner syndrome may be suspected when there are a number of typical physical features observed such as webbed neck, a broad chest and widely spaced nipples. read more

A diagnosis of Turner syndrome is confirmed with special blood tests. The point in life when Turner syndrome is diagnosed will depend on the severity of the condition. A diagnosis of Turner syndrome can be made during prenatal testing. read more

How you learn your child has Turner syndrome may vary. Before birth. Turner syndrome may be suspected by prenatal cell-free DNA screening or certain features may be detected on prenatal ultrasound screening. Prenatal diagnostic testing can confirm the diagnosis. At birth. read more

Turner syndrome (TS), also known as 45,X or 45,X0, is a condition in which a female is partly or completely missing an X chromosome. Signs and symptoms vary among those affected. Often, a short and webbed neck, low-set ears, low hairline at the back of the neck, short stature, and swollen hands and feet are seen at birth. read more