%0 Case Reports
%T 18p Deletion Syndrome With a 45, XY, t (14;18) (p11.1; p11.1), Karyotype.
%A Ashgan B
%A Al-Agha A
%A Alhamdani Y
%A Shazly MA
%J Cureus
%V 16
%N 3
%D 2024 Mar
%M 38576635
暂无%R 10.7759/cureus.55539
%X Monosomy 18p deletion syndrome is a rare genetic disorder. We present an uncommon case of 18p deletion syndrome originating from a unique translocation between chromosomes 14 and 18 in an 11-year-old Saudi male, manifesting various clinical features. This case highlights the importance of understanding the genotype-phenotype correlations of 18p deletion syndrome to aid in the early recognition of the syndrome for its effective diagnosis and management.