hrp0097p1-262 | Fat, Metabolism and Obesity | ESPE2023
Rosmaninho-Salgado Joana
, B. Sousa Sergio
, M. Pires Luis
, Ferreira Susana
, B. Melo Joana
, M. Carreira Isabel
, M. Saraiva Jorge
Background: 16p11.2 microdeletion is most common chromosomal anomaly associated with syndromic obesity. The presence of a large number of flanking segmental duplications/low-copy repeat sequences with a high degree of sequence identity in the short arm of chromosome 16 (16p) leads to recurrent deletions and duplications as a consequence of non-allelic homologous recombination. A recurrent 600kb microdeletion is one of the most frequent genomic imbalances in 16...