Article

Clinical characteristics of a pediatric cohort of patients with combined pituitary insufficiency caused by mutations of the PROP1 gene

2023-07-20

Abstract excerpt

<title>Abstract</title> <p>The most commonly identified genetic cause of combined pituitary deficiency (CPHD) are <italic>PROP1</italic> gene mutations. <bold>The aim</bold> of the study was to compare selected clinical features of patients with CPHD caused by mutations of the <italic>PROP1</italic> gene (CPHD-PROP1) and patients with inborn CPHD of other etiology (CPHD-nonPROP1). <bold>Material and Methods:</bol...

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Literature Corpus work: 4ed0cf6e-f09b-53ea-80f4-195c80bb1203
DOI: 10.21203/rs.3.rs-3152500/v1

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