Non-functioning pituitary adenomas infrequently harbor G-protein gene mutations

2008 ◽  
Vol 31 (11) ◽  
pp. 946-949 ◽  
Author(s):  
R. M. Ruggeri ◽  
L. Santarpia ◽  
L. Curtò ◽  
M. L. Torre ◽  
M. Galatioto ◽  
...  
2011 ◽  
Vol 152 (18) ◽  
pp. 722-730 ◽  
Author(s):  
Judit Dénes ◽  
Márta Korbonits ◽  
Erika Hubina ◽  
Gábor László Kovács ◽  
László Kovács ◽  
...  

Familial pituitary adenomas occur in multiple endocrine neoplasia type 1, Carney complex, as well as in familial isolated pituitary adenoma syndrome. Familial isolated pituitary adenoma syndrome is an autosomal dominant disease with incomplete penetrance. Pituitary adenomas occur in familial setting but without any other specific tumors. In 20-40% of families with this syndrome, mutations have been identified in the aryl hydrocarbon receptor interacting protein gene while in the rest of the families the causative gene or genes have not been identified. Families carrying aryl hydrocarbon receptor interacting protein gene mutations have a distinct phenotype with younger age at diagnosis and a predominance of somatotroph and lactotroph adenomas. Germline mutations of the aryl hydrocarbon receptor interacting protein gene can be occasionally identified in usually young-onset seemingly sporadic cases. Genetic and clinical testing of relatives of patients with aryl hydrocarbon receptor interacting protein gene mutations can lead to earlier diagnosis and treatment at an earlier stage of the pituitary tumor. Orv. Hetil., 2011, 152, 722–730.


1995 ◽  
Vol 80 (5) ◽  
pp. 1702-1705
Author(s):  
E A Williamson ◽  
S J Johnson ◽  
S Foster ◽  
P Kendall-Taylor ◽  
P E Harris

1998 ◽  
Vol 43 (2) ◽  
pp. 297-297 ◽  
Author(s):  
H M Domene ◽  
M Gryngarten ◽  
G Sanso ◽  
S Copelli ◽  
M E Escobar

2005 ◽  
Vol 113 (08) ◽  
Author(s):  
J Szymas ◽  
K Schluens ◽  
W Liebert ◽  
I Petersen

2014 ◽  
Author(s):  
Sandra Rotondi ◽  
Maria Antonietta Oliva ◽  
Vincenzo Esposito ◽  
Luca Ventura ◽  
Felice Giangaspero ◽  
...  

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