[Tumor of the pancreas as the cause of Cushing's syndrome (clinical study)].
Explore the source record for details and available documents.
Biomedical subjects
Publications and source records attributed to N A Zarubina.
Explore the source record for details and available documents.
Explore the source record for details and available documents.
Explore the source record for details and available documents.
Explore the source record for details and available documents.
Explore the source record for details and available documents.
Explore the source record for details and available documents.
Explore the source record for details and available documents.
Explore the source record for details and available documents.
Explore the source record for details and available documents.
Explore the source record for details and available documents.
Explore the source record for details and available documents.
Explore the source record for details and available documents.
Explore the source record for details and available documents.
Explore the source record for details and available documents.
Explore the source record for details and available documents.
Genetic nanism is a widespread phenomenon. Only familial forms constituted 22.8% of the cases of hypophysial and cerebral nanism. A total of 32 patients belonging to 15 families with repeated cases of the disease were examined clinically and electroencephalographically. In genetic hypophysial nanism clinical peculiarities of the disease and the EEG indices were similar within the limits of the same family and showed distinct differences in the patients belonging to different families. The differences are determined chiefly by the level of sex maturation. The EEG in genetic hypophysial nanism was identical to that in the total group of patients with the hypophysial nanism without any organic cerebral pathology. The EEG of the sexually immature patients suffering from nanism was characterized by the immaturity features both in the prepubertal period and in the course of the whole following life, whereas in the patients with a spontaneous sexual development the EEG corresponded to the age criteria at any age. The EEG examination of the patients with hypophysial nanism at the prepubertal period permits to prognosticate their subsequent sexual development.
Explore the source record for details and available documents.
With the aid of insulin-tolerance and arginine tolerance tests (ITT and ATT, respectively) somatotropic function of the hypophysis was assessed in 18 patients with hypophyseal nanism and in 12--with gonad dysgenesis. A marked delay in development and a premature exhaustion of the STH secretion was noted in the patients wiht hypophyseal nanism. In patients with gonad dysgenesis the STH secretion was somewhat redeced during the ITT. A change in the STH secretion was accompanied by a parallel depression of insulin secretion during the ATT. Patients with hypophyseal nanism displayed a correlation between the extent of growth delay and the value of the STH secretion during the ITT (R=0.6, P smaller than 0.05).