Amara Javaid1, Irfan Afzal Mughal2and Muhammad Ismail 1
1. Institute of Biomedical and Genetic Engineering, 24-Mauve Area, G-9/1, Islamabad, Pakistan.
2. HBS Medical and Dental College, Lehtrar Road, Taramri, Islamabad, Pakistan.
Corresponding Author: Amara Javaid, Institute of Biomedical and Genetic Engineering, 24-Mauve Area, G-9/1, Islamabad, Pakistan.
Published Date: 29 April 2025 ; Received Date: 25 March 2025
49, XXXXY syndrome is a rare 1; 85,000-100,000 aneuploidic sex chromosome disorders.
Back-ground:Our study comprises of a male patient born to a non-consanguineous family aged 12 years but the mental age is of 6 years. Low
birth weight was reported with difficulty swallowing. He has moderately low IQ and has several behavioural problems like aggression, shyness
and social awkwardness. He has a history of expressive receptive communication disorder. His developmental milestones were delayed. He has
a history of fits leading to collapse.
Methods: Karyotyping using peripheral blood was carried out to check for any possible chromosomal abnormality.
Conclusion: presence of extra copies of X chromosomes is linked to multiple disorders in the present case. Prenatal amniocentesis would be
of great help for early detection of such syndromes in future
Keywords: 49, XXXXY Syndrome, aneuploidy, sex chromosome, Klinefilter syndrome variant.