| Literature DB >> 28483363 |
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.Entities:
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