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Trisomy 13 (patau syndrome) is a rare genetic condition when an extra copy of chromosome 13 attaches to a pair of chromosomes Other physical symptoms may include Symptoms affect how the face, brain and heart develop, along with several other internal organs.
Trisomy 13, or patau syndrome, is a genetic disorder that affects the development of a baby About 80% of these babies have heart problems, and cleft lip or palate is common Learn about the symptoms, diagnosis, and treatment options.
Trisomy 13 is a serious genetic condition
It is also sometimes called patau syndrome Not all babies with trisomy 13 will have the same differences or challenges Some common things that can be caused by trisomy 13 include: Treatment of patau syndrome focuses on the particular physical problems with which each child is born
Many infants have difficulty surviving the first few days or weeks due to severe neurological problems or complex heart defects. Trisomy 13, also called patau syndrome, is a chromosomal condition associated with severe intellectual disability and physical abnormalities in many parts of the body. Key takeaways trisomy 13 (patau syndrome) is a rare genetic condition caused by an extra chromosome 13, leading to a range of developmental, physical, and neurological challenges Common symptoms include cleft lip and palate, heart defects, brain malformations, and intellectual disabilities.
Patau syndrome, or trisomy 13, is a genetic disease that impacts the development of the heart, facial features and brain
Babies are typically born with nervous system malformations, a cleft lip and a low birth weight Learn more about the symptoms of patau syndrome, what causes it, and how it's. Patau syndrome, also known as trisomy 13, is a genetic disorder characterized by a specific set of symptoms including brain abnormalities, cleft palate, hare lip, unusual hand lines, extra thumbs, additional fingers or toes, and birthmarks caused by blood vessels. Babies with patau's syndrome can have a wide range of health problems
Their growth in the womb is often restricted, resulting in a low birth weight, and 8 out of 10 will be born with severe heart defects The brain often does not divide into 2 halves This is known as holoprosencephaly. Babies born with trisomy 13 often have a low birth weight and brain structure problems that affect facial development
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