hrp0097p1-546 | Pituitary, Neuroendocrinology and Puberty | ESPE2023
Eren Erdal
, Tezcan Unlu Havva
, Denkboy Ongen Yasemin
, Cecener Gulsah
Introduction: Congenital multiple pituitary hormone deficiency (CMPHD) is a clinical condition that manifests in the early years of life. In most cases, pituitary stalk interruption syndrome (PSIS) can be detected by MR imaging. The current study presents a case with a novel candidate pathogenic gene Semaphorin 3A (SEMA3A) in CMPHD by whole-exome sequencing (WES).Materials and Methods: Genomic DNA was extracted from the ...