hrp0089p3-p259 | Growth & Syndromes P3 | ESPE2018
Leka-Emiri Sofia
, Petrou Vassilios
, Manolakos Emmanouil
, Fotinou Aspasia
, Thomaidis Loretta
, Vlachopapadopoulou Elpis
, Michalacos Stefanos
Background: To date, six cases of 17p13.1 microduplications have been described in the literature. Intellectual disability is the core feature, together with minor facial dysmorphisms and obesity later in life, but a characteristic phenotype for 17p13.1 microduplication has not been delineated.Objective and hypothesis: We describe a young patient with a 422 Kb microduplication maternally inherited in 17p13.1, affected by mild intellectual disability and ...