Nguyen ThiThuyAn, McDonnell Ciara M, Zacharin Margaret R
Department ofPaediatrics, University of Melbourne, Australia.
J Pediatr Endocrinol Metab. 2005 Oct;18(10):1013-7. doi: 10.1515/jpem.2005.18.10.1013.
A 14 year-old girl was found to have a deletion of the distal segment of chromosome 3 [46,XX,Del(3)(q28-29)]. The main features of this presentation were mild intellectual disability, facial dysmorphism, short stature, kypho-scoliosis, and primary ovarian failure, an association that has not been described before in association with chromosome 3 deletion. The phenotype and presentation are compared with those of previous case reports.