Combined pituitary hormone deficiency caused by PROP1 mutations: update 20 years post-discovery

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PROP1 gene analysis in Portuguese patients with combined pituitary hormone deficiency.

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Molecular analysis of PROP1, PIT1, HESX1, LHX3, and LHX4 shows high frequency of PROP1 mutations in patients with familial forms of combined pituitary hormone deficiency.

UNLABELLED Combined Pituitary Hormone Deficiency (CPHD) is a prevalent disease in Neuroendocrinology services. The genetic form of CPHD may originate from mutations in pituitary transcription factor (PTF) genes and the pituitary image in these cases may give a clue of what PTF is most probably mutated: defects in LHX4 are usually associated with ectopic posterior pituitary (EPP); defects in LHX...

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ژورنال

عنوان ژورنال: Archives of Endocrinology and Metabolism

سال: 2019

ISSN: 2359-3997,2359-4292

DOI: 10.20945/2359-3997000000139