Literature DB >> 28483363

AIP mutations and gigantism.

Liliya Rostomyan1, Iulia Potorac1, Pablo Beckers2, Adrian F Daly1, Albert Beckers3.   

Abstract

AIP mutations are rare in sporadic acromegaly but they are seen at a higher frequency among certain specific populations of pituitary adenoma patients (pituitary gigantism cases, familial isolated pituitary adenoma (FIPA) kindreds, and patients with macroadenomas who are diagnosed ≤30 years). AIP mutations are most prevalent in patients with pituitary gigantism (29% of this group were found to have mutations in AIP gene). These data support targeted genetic screening for AIP mutations/deletions in these groups of pituitary adenoma patients. Earlier diagnosis of AIP-related acromegaly-gigantism cases enables timely clinical evaluation and treatment, thereby improving outcomes in terms of excessive linear growth and acromegaly comorbidities.
Copyright © 2017 Elsevier Masson SAS. All rights reserved.

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Keywords:  Adénome hypophysaire; Adénome hypophysaire familial isolé (FIPA); Aryl hydrocarbon receptor interacting protein (AIP) gene; Familial isolated pituitary adenoma (FIPA); Gigantism; Gigantisme; Gène de aryl hydrocarbon receptor interacting protein (AIP); Pituitary adenoma

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Year:  2017        PMID: 28483363     DOI: 10.1016/j.ando.2017.04.012

Source DB:  PubMed          Journal:  Ann Endocrinol (Paris)        ISSN: 0003-4266            Impact factor:   2.478


  1 in total

Review 1.  Giant pituitary adenoma: histological types, clinical features and therapeutic approaches.

Authors:  Pedro Iglesias; Víctor Rodríguez Berrocal; Juan José Díez
Journal:  Endocrine       Date:  2018-06-16       Impact factor: 3.633

  1 in total

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