Endocrine abnormalities are known to affect patients with Fabry disease (FD). Pituitary gland theoretically represents an ideal target for FD because of high vascularization and low proliferation rate. We explored pituitary morphology and function in a cohort of FD patients through a prospectic, monocentric study at an Academic Tertiary Center. The study population included 28 FD patients and 42 sex and age-matched normal subjects. The protocol included a contrast enhancement pituitary MRI, the assessment of pituitary hormones, anti-pituitary, and anti-hypothalamus antibodies. At pituitary MRI, an empty sella was found in 11 (39%) FD patients, and in 2 (5%) controls (p < 0.001). Pituitary volume was significantly smaller in FD than in contr...
peer reviewedContext: McCune Albright syndrome (MAS) is a clinical association of endocrine and non-...
Fabry disease (FD) is a lysosomal storage disorder where deficient or completely absent activity of ...
Anterior Pituitary Hormone Deficiencies may be due to any lesion in this anatomical region, most com...
Endocrine abnormalities are known to affect patients with Fabry disease (FD). Pituitary gland theore...
Endocrine abnormalities are known to affect patients with Fabry disease (FD). Pituitary gland theore...
BACKGROUND: Fabry disease (FD) is a genetic disorder caused by lysosomal alpha-galactosidase-A defi...
BACKGROUND: Fabry disease (FD) is a genetic disorder caused by lysosomal alpha-galactosidase-A def...
CONTEXT Fabry Disease (FD) is a rare X-linked storage disease characterised by a-galactosidase A ...
OBJECTIVE: Primary empty sella (PES) is a frequent anatomical condition rarely causing pituitary dys...
AM: Patients with Fabry disease (FD), a genetic disorder caused by lysosomal a-galactosidase-A enzym...
BACKGROUND : Fanconi anemia (FA) is phenotypically diverse, hereditary condition associated with bon...
Abstract BACKGROUND: Anderson-Fabry disease (AFD) is an inborn lysosomal enzymopathy resulting from...
BackgroundFabry disease is caused by a deficient or an absent alfa‐galactosidase A activity and is a...
Fabry disease (FD) is an inherited metabolic disorder caused by partial or full inactivation of the ...
peer reviewedContext: McCune Albright syndrome (MAS) is a clinical association of endocrine and non-...
Fabry disease (FD) is a lysosomal storage disorder where deficient or completely absent activity of ...
Anterior Pituitary Hormone Deficiencies may be due to any lesion in this anatomical region, most com...
Endocrine abnormalities are known to affect patients with Fabry disease (FD). Pituitary gland theore...
Endocrine abnormalities are known to affect patients with Fabry disease (FD). Pituitary gland theore...
BACKGROUND: Fabry disease (FD) is a genetic disorder caused by lysosomal alpha-galactosidase-A defi...
BACKGROUND: Fabry disease (FD) is a genetic disorder caused by lysosomal alpha-galactosidase-A def...
CONTEXT Fabry Disease (FD) is a rare X-linked storage disease characterised by a-galactosidase A ...
OBJECTIVE: Primary empty sella (PES) is a frequent anatomical condition rarely causing pituitary dys...
AM: Patients with Fabry disease (FD), a genetic disorder caused by lysosomal a-galactosidase-A enzym...
BACKGROUND : Fanconi anemia (FA) is phenotypically diverse, hereditary condition associated with bon...
Abstract BACKGROUND: Anderson-Fabry disease (AFD) is an inborn lysosomal enzymopathy resulting from...
BackgroundFabry disease is caused by a deficient or an absent alfa‐galactosidase A activity and is a...
Fabry disease (FD) is an inherited metabolic disorder caused by partial or full inactivation of the ...
peer reviewedContext: McCune Albright syndrome (MAS) is a clinical association of endocrine and non-...
Fabry disease (FD) is a lysosomal storage disorder where deficient or completely absent activity of ...
Anterior Pituitary Hormone Deficiencies may be due to any lesion in this anatomical region, most com...