Pituitary deficiency due to empty sella turcica syndrome

Orpha code: 91354OMIM code:

Definicja

A rare pituitary deficiency characterized by herniation of the subarachnoid space into the sella turcica, resulting in flattening of the pituitary gland and endocrine dysfunction. Most common endocrine abnormalities are hyperprolactinemia and growth hormone deficit. Clinical symptoms are highly variable and include headaches, irregular menstruation, galactorrhea, obesity, and visual disturbances, among others.

Disease data
Klasyfikacja

Disease

Synonimy
Hypopituitarism due to empty sella turcica syndrome
Hypopituitarism due to empty sella turcica syndrome
Kod ORPHA
91354
Kod OMIM
-
Kod ICD10
E23.0
Kod ICD11
-

No additional description.

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