Results 31 to 40 of about 55,893 (295)

Late diagnosis of primary chronic adrenal insufficiency in the framework of autoimmune polyglandular syndrome type 2. Clinical observation

open access: yesЛечащий Врач, 2023
Chronic adrenal insufficiency is caused by insufficient secretion of hormones by the adrenal cortex due to dysfunction of one or more links of the hypothalamic-pituitary-adrenal system.
V. G. Chobitko, A. P. Belova
doaj   +1 more source

Adrenal crises: perspectives and research directions [PDF]

open access: yes, 2017
Adrenal crises (AC) are life-threatening complications of adrenal insufficiency (AI). These events have an estimated incidence of between 5 and 10 ACs/100 patient years (PY) and are responsible for some of the increased morbidity and excess mortality ...
Falhammar, H, Rushworth, R, Torpy, D
core   +2 more sources

Primary adrenal lymphoma: Differential involvement with varying adrenal function

open access: yesIndian Journal of Endocrinology and Metabolism, 2011
Primary adrenal Non-Hodgkin′s lymphoma is rare. The symptoms of the disease and response to treatment are variable depending on the type of lymphoma, tumor size, and presence of adrenal insufficiency.
Shiekh Aejaz Aziz   +4 more
doaj   +1 more source

GNAS mutation is an unusual cause of primary adrenal insufficiency: a case report

open access: yesBMC Pediatrics, 2022
Background Primary adrenal insufficiency in children has non-specific and extensive clinical features, so the diagnosis of its etiology is complex and challenging.
Yajie Tong   +3 more
doaj   +1 more source

Reversible dilated cardiomyopathy as a complication of adrenal cortex insufficiency: a case report

open access: yesJournal of Medical Case Reports, 2018
Background Cardiovascular manifestations associated with Addison’s disease are previously documented. We described a case of an 11-year-old girl who developed dilated cardiomyopathy as a complication to Addison’s disease.
Mohammad Alkhateeb   +3 more
doaj   +1 more source

Primary adrenal insufficiency in adults: 150 years after Addison [PDF]

open access: yes, 2004
Thomas Addison first described, 150 years ago, a clinical syndrome characterized by salt-wasting and skin hyperpigmentation, associated with a destruction of the adrenal gland.
Alvarenga, Daniela B. de   +7 more
core   +4 more sources

A rare occurrence of central precocious puberty in adrenal hypoplasia congenita

open access: yesSri Lanka Journal of Medicine, 2020
AHC (X-linked adrenal hypoplasia congenita) is a rare cause of adrenal insufficiency due to mutations in the DAX1 gene. It traditionally causes hypogonadotropic hypogonadism.
Rajesh Joshi, Karthik Shroff
doaj   +1 more source

Mutational analysis of DAX1 in patients with hypogonadotropic hypogonadism or pubertal delay [PDF]

open access: yes, 1999
Although delayed puberty is relatively common and often familial, its molecular and pathophysiologic basis is poorly understood. In contrast, the molecular mechanisms underlying some forms of hypogonadotropic hypogonadism (HH) are clearer, following the ...
Achermann, JC   +12 more
core   +1 more source

Glucocorticoid therapy for adrenal insufficiency: nonadherence, concerns and dissatisfaction with information [PDF]

open access: yes, 2016
Objective: Appropriate self‐management of glucocorticoid therapy (GC) is crucial for patients with adrenal insufficiency (AI). We aimed to describe patients’ self‐reported nonadherence to GC, evaluate perceived doubts about need for GC, concerns about ...
Carroll, P.   +3 more
core   +2 more sources

The hepatoadrenal syndrome: A common yet unrecognized clinical condition [PDF]

open access: yes, 2005
Objective: Adrenal failure is common in critically ill patients, particularly those with sepsis. As liver failure and sepsis are both associated with increased circulating levels of endotoxin and proinflammatory mediators and reduced levels of apoprotein-
Acton   +51 more
core   +1 more source

Home - About - Disclaimer - Privacy