Comparison of clinical characteristics of a pediatric cohort with combined pituitary hormone deficiency caused by mutation of the PROP1 gene or of other origins

CONCLUSION: Patients with the PROP1 mutations present a clinical picture significantly different from that of other forms of congenital hypopituitarism. Certain specific clinical results may lead to the successful identification of children requiring diagnostics for the PROP1 gene mutation.PMID:38147295 | DOI:10.1007/s42000-023-00510-1

Source: Hormones - December 26, 2023 Category: Endocrinology Authors: Agata Zygmunt-G órska Ma łgorzata Wójcik None AleksandraGilis-Januszewska Anna Starmach Miros ław Bik-Multanowski Jerzy B Starzyk Source Type: research