%0 Case Reports
%T A Rare Cytogenetic Variant of Monosomy 18p Syndrome as a Consequence of Whole-Arm Translocation between Chromosomes 13 and 18.
%A Safavi M
%A Haghi Ashtiani MT
%A Badv RS
%A Azari-Yam A
%A Vasei M
%J Arch Iran Med
%V 22
%N 10
%D 10 2019 1
%M 31679365
%F 3.138
%X Monosomy 18p syndrome is one of the prototypical examples of autosomal terminal deletions. This deletion can be the consequence of de novo deletions, malsegregation of a balanced parental translocation, cryptic subtelomeric deletions or ring chromosome 18. The present case is a rare cytogenetic variant of monosomy 18 as a consequence of whole-arm translocation between chromosomes 13 and 18 which has been reported only three times previously.