Trisomy 13

Trisomy 13 syndrome: Condition with three rather than the normal two chromosomes #13. Children born with this syndrome have multiple malformations and mental retardation due to the extra chromosome #13.
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Trisomy 13 can be diagnosed prenatally by amniocentesis with chromosome studies of the amniotic cells. Trisomy 13 mosaicism and partial trisomy 13 also occur.
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Trisomy 13 occurs in about 1 out of every 5,000 live births. It is a syndrome with multiple abnormalities, many of which are not compatible with more than a few months of life.
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Patau syndrome (trisomy 13 syndrome): A syndrome characterized by multiple malformations, commonly including scalp defects, hemangiomas (blood vessel malformations) of the face and nape of the neck, cleft lip and palate, ...
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Trisomy 13 is also called "Patau syndrome," named after the physician who first described the disorder. Trisomy 13 is seen in about one in 7500 to one in 10,000 births.
What causes trisomy 18 and trisomy 13?
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The majority of congenital heart diseases occur as an isolated defect and are not associated with other diseases. However, they can also be a part of various genetic and chromosomal syndromes, such as Down syndrome, trisomy 13, Turner's syndrome, ...
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sweaty feet can also predispose you to having an ingrown toenail. Ingrown toenails are also more common in people with certain diseases, including hyperthyroidism, diabetes mellitus, acromegaly and some congenital conditions, like trisomy 13 syndrome.
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