FAMILIAL PITUITARY ADENOMA / PROLACTINOMA: CLINICAL EXOME PANEL (Sec. & CNVs) – 15 genes
LabGenetics
Delivery time
3-4 weeks
Sample
Blood
The Familial Pituitary Adenoma/Prolactinoma Panel is designed for the genetic study of patients with hereditary or multiple pituitary adenomas, including prolactinomas, somatotropinomas, corticotropinomas, and non-functioning adenomas. These alterations may be associated with tumor predisposition syndromes such as multiple endocrine neoplasia type 1 (MEN1), Carney complex, or syndromes caused by AIP mutations. Clinical exome sequencing and CNV detection allow for the identification of pathogenic variants that explain familial susceptibility, contributing to accurate molecular diagnosis, genetic counseling, and personalized clinical management. Genes analyzed: AIP, MEN1, CDKN1B, GNAS, PRKAR1A, SDHA, SDHB, SDHC, SDHD, and others. You can consult the complete list of analyzed genes by contacting Genotica.
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