ea0090ep696 | Pituitary and Neuroendocrinology | ECE2023
Perepelova Margarita
, Dzeranova Larisa
, Shutova Aleksandra
, Lepeshkina Lyudmila
, Pigarova Ekaterina
, Azizyan Vilen
, Akopyan Pavel
, Przhiyalkovskaya Elena
Background: Acromegaly is an orphan neuroendocrine disease characterized by a variety of complications. Due to slow symptom progression acromegalic patients often are involved in growth hormone complications correction for a long time instead of search for main cause of these multiple disorders. A view on conductive hearing loss in acromegaly in literature is contradictory. The low incidence of hearing in acromegaly, compared with other complications, is presumably due to the ...