Literature DB >> 19834305

[Evaluation of pituitary imaging in patients with prop-1 gene mutation].

Natalija Tkacenko1, Danute Lasiene, Silvija Jakstiene, Algidas Basevicius, Rasa Verkauskiene.   

Abstract

The most common genetically determined cause of multiple pituitary hormone deficiency is PROP-1 gene mutation. PROP-1 is a transcription factor involved in the development of pituitary gland and affects hormonal synthesis of anterior pituitary. The aim of our study was to evaluate radiological aspects of the pituitary region in patients with PROP-1 gene mutation. Pituitary imaging studies were performed in 12 patients with a confirmed PROP-1 gene mutation. Pituitary hyperplasia was found in 5 (42%) and pituitary hypoplasia in 4 (33%) patients. Changes in pituitary size were not associated with the type of PROP-1 gene mutation.

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Year:  2009        PMID: 19834305

Source DB:  PubMed          Journal:  Medicina (Kaunas)        ISSN: 1010-660X            Impact factor:   2.430


  2 in total

1.  Congenital hypopituitarism: how to select the patients for genetic analyses.

Authors:  Giuseppe Crisafulli; Tommaso Aversa; Giuseppina Zirilli; Filippo De Luca; Romina Gallizzi; Malgorzata Wasniewska
Journal:  Ital J Pediatr       Date:  2018-04-06       Impact factor: 2.638

2.  Genetic causes of hypopituitarism.

Authors:  Katherine Parkin; Ritika Kapoor; Ravindra Bhat; Anne Greenough
Journal:  Arch Med Sci       Date:  2019-12-31       Impact factor: 3.318

  2 in total

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