First report on chromosomal abnormalities in Eastern Morocco: Identification of a new case of a de novo partial trisomy 13q using single-nucleotide polymorphism array

CONCLUSION: This study provided the first report on chromosomal abnormalities in Eastern Morocco and it enriched the phenotype spectrum of partial trisomy 13q and further confirmed the genotype-phenotype correlations. Furthermore, these findings justify the need to set up microarray comparative genomic hybridization techniques in Morocco for better genetic diagnosis.PMID:38262863 | DOI:10.1016/j.arcped.2023.10.002

Source: Archives de Pediatrie - January 23, 2024 Category: Pediatrics Authors: Manal Elidrissi Errahhali Mounia Elidrissi Errahhali Sara Ramdani Saida Lhousni Noufissa Benajiba Maria Rkain Abdeladim Babakhouya Aziza Elouali Ayad Ghanam Rim Amrani Sahar Messaoudi Anass Ayyad Bouchra Oneib Ahmed Mimouni Hanane Saadi Sanae Allaoui Mery Source Type: research