Complete
trisomy 22 occurs when an extra (third) copy of chromosome 22 is
present in every cell of the body, where there should normally
only be two copies. Cases of complete (or full) trisomy 22 are
very rare. Many affected individuals with complete trisomy 22
have a shortened life span and it is rare to find many articles
in the literature highlighting cases with this condition.
Complete trisomy 22 is the second most common finding in
miscarriages after trisomy 16.
Early reports of complete trisomy 22 are thought to represent unbalanced translocation 11/22 (Emanuel Syndrome) or mosaicism. Our group is aware of a few reports of people with full trisomy 22 living for many years longer than can be identified in medical journals. There has been a shift in offering surgical intervention for children born with this condition, offering opportunity for extended survival rates (Phung, et al 2023). Due to the limited information on trisomy 22, it may be helpful for parents to look to the work of SOFT - Support Organization for Trisomy, and children born with trisomies 13 and 18. A statement by the SOFT Board of Directors released December 14th, 2023 discusses terminology used to describe these trisomies.
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Affiliate member, Canadian Organization for Rare Disorders