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Article

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

Hormones (Athens, Greece) - 1 Mar 2024

Zygmunt-Górska Agata, Wójcik Małgorzata, Gilis-Januszewska Aleksandra, Starmach Anna, Bik-Multanowski Mirosław, Starzyk Jerzy B

Abstract excerpt

The most commonly identified genetic cause of combined pituitary hormone deficiency (CPHD) is PROP1 gene mutations. The aim of the study was to compare selected clinical features of patients with CPHD caused by variants of the PROP1 gene (CPHD-PROP1) and patients with inborn CPHD of other etiology (CPHD-nonPROP1). MATERIAL AND METHODS: The retrospective analysis included childhood medical records of 74 patients...

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PMID: 38147295
DOI: 10.1007/s42000-023-00510-1
PMCID: PMC10847174

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