Turner syndrome is a rare genetic disorder found in some women and people assigned female at birth. It can cause short stature and a range of health issues including heart defects, learning ...

Risk Factors Turner syndrome is not something that is inherited from families, but is the result of genetic changes that occur by chance. Therefore, there are no specific risk factors that can ...

Turner syndrome is a chromosomal disorder that affects females only. Read about its causes, signs, diagnosis, treatment, and possible complications.

If your doctor suspects that your child has Turner syndrome, a genetic test will typically be done to analyze their chromosomes. (4) This test is usually done with a blood sample, although your ...

Rett syndrome is a rare developmental disorder, most often due to a mutation in the MECP2 gene on the X chromosome, but it’s not usually inherited. Advances in genetics have launched a new era ...

Dr. Hurst is a physician for the UAB Undiagnosed Disease program, Turner syndrome clinic, and general genetics clinic, and she provides hospital consultations for inpatients at UAB and Children ...

Fraser syndrome is a genetic disorder, which means that it occurs due to mutations in the genes. The genes resulting in Fraser syndrome are the FRAS1, FREM2, and GRIP1 genes.

This story was excerpted from Adam Berry’s Rays Beat newsletter. To read the full newsletter, click here. And subscribe to get it regularly in your inbox. ST. PETERSBURG -- For Pete Fairbanks, every ...

What is Turner syndrome? Turner syndrome also known as gonadal dysgenesis is a genetic disorder that affects only girls. Human beings generally have 23 pairs of chromosomes – a total of 46 chromosomes ...

Turner syndrome is a congenital disorder affecting females caused by a missing or partially missing X chromosome. It affects one of every 2,500 female babies, causing medical and developmental ...