hrp0082p3-d3-912 | Pituitary (1) | ESPE2014

Screening for SOX2 Mutations in Bulgarian Patients with Congenital Hyposomatotropism: First Results

Aroyo Ani , Stoeva Iva , Dacheva Daniela , Kaneva Radka , Mitkova Atanaska , Oscar Alexander , Haikin Vassil , Mitev Vanio

Background: The transcription factor (TF) SOX2 is expressed early in the embryological development and is essential for the development of many structures like neural system, pituitary gland, eyes, ears, esophagus, and gonads. The most common clinical manifestations of mutations in the SOX2 gene are eye abnormalities (anophthalmia/microphthalmia, coloboma, nystagm, and refractive errors) and hypopituitarism (deficiency of gonadotropic, GH, TSH, and ACTH). Molecular genetic stu...