RARE CASE OF ENDOGENOUS FAMILY HYPERCORTICISM (CLINICAL CASE)
We described a case of an endogenous hypercorticism in 18-years old patient with Itsenko - Cushing syndrome which was caused by a hormonally active adrenal tumor of the left adrenal gland. In a clinical picture of a disease the following symptoms dominated: arterial hypertension, increase in body we...
Saved in:
Main Authors: | V. F. Sobotovich, Y. A. Privalov, L. K. Kulikov |
---|---|
Format: | article |
Language: | RU |
Published: |
Scientific Сentre for Family Health and Human Reproduction Problems
2017
|
Subjects: | |
Online Access: | https://doaj.org/article/46b4ce64c1304c9ba612bea73bff8c07 |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Similar Items
-
Tuberous Sclerosis: A Case Report with Oral Manifestation
by: Curi,Marcos Martins, et al.
Published: (2014) -
Tríada de Carney. Una rara asociación de tumores infrecuentes: Caso clínico
by: Vega,Jorge, et al.
Published: (2017) -
Síndrome de Cushing durante el embarazo: manifestaciones cutáneas secundarias a un tumor suprarrenal
by: Molgó N,Montserrat, et al.
Published: (2013) -
Resultados del trasplante renal en portadores de ríñones poliquísticos
by: Vega,Jorge, et al.
Published: (2012) -
Síndrome de Cushing provocado por carcinoma suprarrenal gigante. Caso clínico
by: Zapata Pizarro,Antonio, et al.
Published: (2020)