Medical Definition of Trisomy 18 syndrome

1. There are three instead of the normal two chromosomes 18. Children with this condition have multiple malformations and mental retardation due to the extra chromosome 18. The children characteristically have low birth weight, small head (microcephaly), small jaw (micrognathia), malformations of the heart and kidneys, clenched fists with abnormal finger positioning, and malformed feet. The mental retardation is profound with the iq too low to even test. Nineteen out of 20 (95%) of these children die before their first birthday. The condition is also called edwards syndrome in honor of the british physician and geneticist john edwards who discovered the extra chromosome in 1960. (12 Dec 1998)

Lexicographical Neighbors of Trisomy 18 Syndrome

trisoctahedra
trisoctahedron
trisoctahedrons
trisodium
trisodium orthophosphate
trisodium phosphate
trisoligonucleotide
trisoligonucleotides
trisome
trisomes
trisomic
trisomics
trisomies
trisomy
trisomy 18 syndrome (current term)
trisomy 20 syndrome
trisomy 21 syndrome
trisomy 8 syndrome
trisomy C syndrome
trispaston
trispectra
trispectrum
trisphosphate
trisphosphates
trisplanchnic
trispyrazolylborate

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