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Photo Gallery. Here are photos of the children and young adults with rare trisomy conditions who have graced these web pages since September 2005. Photos Needed - One of the ways that the TRIS Project disseminates information about children and young adults with rare trisomy syndromes is by electronic and print materials.
Trisomy 13 (Patau syndrome) and Trisomy 18 (Edwards syndrome) are genetic disorders that include health problems that affect almost every organ of the body. They are fatal diagnoses — more...
Trisomy 13 (Patau syndrome) is a rare genetic condition that occurs when the 13th chromosome appears three times (trisomy) instead of two times in a person’s DNA. Trisomy 13 affects the development of the face, brain and heart, along with physical growth abnormalities throughout a child’s body.
Browse 17 authentic trisomy 13 stock photos, high-res images, and pictures, or explore additional patau syndrome or trisomy 18 stock images to find the right photo at the right size and resolution for your project.
If your baby has trisomy 13, they may have serious mental and physical problems. It can be found in your first trimester of pregnancy. There's no cure for trisomy 13. But there are treatments...
Trisomy 13 is a serious genetic condition that occurs when there are 3 copies of chromosome 13 instead of the usual 2. Learn about symptoms, diagnosis and outlook.
Patau syndrome is the result of trisomy 13, meaning each cell in the body has three copies of chromosome 13 instead of the usual two. A small percentage of cases occur when only some of the body's cells have an extra copy; such cases are called mosaic trisomy 13.
Learn about Patau syndrome, or Trisomy 13, including its prevalence, symptoms, diagnosis, and treatment.
Trisomy 13 is an aneuploidy (less or more than 46 chromosomes) in which three copies of chromosome 13—instead of the typical two—are present. Complete, mosaic, and partial forms of trisomy 13 exist.
Trisomy 13 is caused by an extra chromosome 13. Infants are typically small and often have major brain, eye, face, and heart defects. Tests can be done before or after birth to confirm the diagnosis.